Linked Data
ClinVar Variation Id:
298860
ClinVar RCV Id:
RCV000367311
dbSNP Id:
rs751292868
ExAC:
10:112724817 T / C
gnomAD v2:
10-112724817-T-C
gnomAD v4:
10-110965059-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.110965059T>C , CM000672.2:g.110965059T>C | GRCh38 |
| NC_000010.10:g.112724817T>C , CM000672.1:g.112724817T>C | GRCh37 |
| NC_000010.9:g.112714807T>C | NCBI36 |
| NG_028922.1:g.50517T>C , LRG_753:g.50517T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000265277.10:c.701T>C | ENSP00000265277.5:p.Ile234Thr | |
| ENST00000451838.2:c.-242-35356T>C | ENSP00000408275.2:n.-242-35356T>C | |
| ENST00000480155.2:n.937T>C | ||
| ENST00000685059.1:c.701T>C | ENSP00000510210.1:p.Ile234Thr | |
| ENST00000685613.1:c.701T>C | ENSP00000510564.1:p.Ile234Thr | |
| ENST00000687592.1:n.1000T>C | ||
| ENST00000688928.1:c.701T>C | ENSP00000509273.1:p.Ile234Thr | |
| ENST00000689118.1:c.701T>C | ENSP00000510554.1:p.Ile234Thr | |
| ENST00000689300.1:c.701T>C | ENSP00000510639.1:p.Ile234Thr | |
| ENST00000689997.1:c.-380-20569T>C | ENSP00000510700.1:n.-380-20569T>C | |
| ENST00000691151.1:n.993T>C | ||
| ENST00000691369.1:c.701T>C | ENSP00000509754.1:p.Ile234Thr | |
| ENST00000691441.1:c.701T>C | ENSP00000509686.1:p.Ile234Thr | |
| ENST00000691903.1:c.701T>C | ENSP00000510314.1:p.Ile234Thr | |
| ENST00000692776.1:c.701T>C | ENSP00000508524.1:p.Ile234Thr | |
| ENST00000369452.9:c.701T>C MANE Select | ENSP00000358464.5:p.Ile234Thr | |
| ENST00000265277.9:c.701T>C | ENSP00000265277.5:p.Ile234Thr | |
| ENST00000369452.8:c.701T>C | ENSP00000358464.4:p.Ile234Thr | |
| ENST00000451838.1:c.209T>C | ENSP00000408275.1:p.Ile70Thr | |
| ENST00000489390.1:n.56-35356T>C | ||
| ENST00000497305.1:n.28T>C | ||
| NM_001269039.1:c.701T>C | NP_001255968.1:p.Ile234Thr | |
| NM_007373.3:c.701T>C , LRG_753t1:c.701T>C | NP_031399.2:p.Ile234Thr | |
| XM_011540216.1:c.-380-20569T>C | XP_011538518.1:n.-380-20569T>C | |
| NM_001269039.2:c.701T>C | NP_001255968.1:p.Ile234Thr | |
| NM_001324336.1:c.701T>C | NP_001311265.1:p.Ile234Thr | |
| NM_001324337.1:c.701T>C | NP_001311266.1:p.Ile234Thr | |
| NR_136749.1:n.116-20569T>C | ||
| NM_007373.4:c.701T>C MANE Select | NP_031399.2:p.Ile234Thr | |
| NM_001269039.3:c.701T>C | NP_001255968.1:p.Ile234Thr | |
| NM_001324336.2:c.701T>C | NP_001311265.1:p.Ile234Thr | |
| NM_001324337.2:c.701T>C | NP_001311266.1:p.Ile234Thr | |
| NR_136749.2:n.55-20569T>C |