Linked Data
ClinVar Variation Id:
139108
dbSNP Id:
rs146147503
ExAC:
10:112769023 C / T
gnomAD v2:
10-112769023-C-T
gnomAD v3:
10-111009265-C-T
gnomAD v4:
10-111009265-C-T
ERepo:
CA293482/MONDO:0021060/004
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.111009265C>T , CM000672.2:g.111009265C>T | GRCh38 |
| NC_000010.10:g.112769023C>T , CM000672.1:g.112769023C>T | GRCh37 |
| NC_000010.9:g.112759013C>T | NCBI36 |
| NG_028922.1:g.94723C>T , LRG_753:g.94723C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000265277.10:c.1164C>T | ENSP00000265277.5:p.Asn388= | |
| ENST00000451838.2:c.219C>T | ENSP00000408275.2:p.Asn73= | |
| ENST00000685059.1:c.1302C>T | ENSP00000510210.1:p.Asn434= | |
| ENST00000685613.1:c.*298C>T | ENSP00000510564.1:n.*298C>T | |
| ENST00000687592.1:n.1601C>T | ||
| ENST00000688928.1:c.1302C>T | ENSP00000509273.1:p.Asn434= | |
| ENST00000689118.1:c.1302C>T | ENSP00000510554.1:p.Asn434= | |
| ENST00000689300.1:c.1302C>T | ENSP00000510639.1:p.Asn434= | |
| ENST00000689997.1:c.219C>T | ENSP00000510700.1:p.Asn73= | |
| ENST00000691369.1:c.1302C>T | ENSP00000509754.1:p.Asn434= | |
| ENST00000691441.1:c.1302C>T | ENSP00000509686.1:p.Asn434= | |
| ENST00000691903.1:c.1302C>T | ENSP00000510314.1:p.Asn434= | |
| ENST00000692776.1:c.1302C>T | ENSP00000508524.1:p.Asn434= | |
| ENST00000369452.9:c.1302C>T MANE Select | ENSP00000358464.5:p.Asn434= | |
| ENST00000265277.9:c.1164C>T | ENSP00000265277.5:p.Asn388= | |
| ENST00000369452.8:c.1302C>T | ENSP00000358464.4:p.Asn434= | |
| ENST00000451838.1:c.672C>T | ENSP00000408275.1:p.Asn224= | |
| ENST00000489390.1:n.516C>T | ||
| NM_001269039.1:c.1164C>T | NP_001255968.1:p.Asn388= | |
| NM_007373.3:c.1302C>T , LRG_753t1:c.1302C>T | NP_031399.2:p.Asn434= | |
| XM_011540216.1:c.219C>T | XP_011538518.1:p.Asn73= | |
| NM_001269039.2:c.1164C>T | NP_001255968.1:p.Asn388= | |
| NM_001324336.1:c.1302C>T | NP_001311265.1:p.Asn434= | |
| NM_001324337.1:c.1302C>T | NP_001311266.1:p.Asn434= | |
| NR_136749.1:n.714C>T | ||
| NM_007373.4:c.1302C>T MANE Select | NP_031399.2:p.Asn434= | |
| NM_001269039.3:c.1164C>T | NP_001255968.1:p.Asn388= | |
| NM_001324336.2:c.1302C>T | NP_001311265.1:p.Asn434= | |
| NM_001324337.2:c.1302C>T | NP_001311266.1:p.Asn434= | |
| NR_136749.2:n.653C>T |