Linked Data
ClinVar Variation Id:
1761127
ClinVar RCV Id:
RCV002416642
dbSNP Id:
rs765714933
ExAC:
10:112724194 G / A
gnomAD v2:
10-112724194-G-A
gnomAD v4:
10-110964436-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.110964436G>A , CM000672.2:g.110964436G>A | GRCh38 |
| NC_000010.10:g.112724194G>A , CM000672.1:g.112724194G>A | GRCh37 |
| NC_000010.9:g.112714184G>A | NCBI36 |
| NG_028922.1:g.49894G>A , LRG_753:g.49894G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000265277.10:c.78G>A | ENSP00000265277.5:p.Lys26= | |
| ENST00000451838.2:c.-242-35979G>A | ENSP00000408275.2:n.-242-35979G>A | |
| ENST00000480155.2:n.314G>A | ||
| ENST00000685059.1:c.78G>A | ENSP00000510210.1:p.Lys26= | |
| ENST00000685613.1:c.78G>A | ENSP00000510564.1:p.Lys26= | |
| ENST00000687592.1:n.377G>A | ||
| ENST00000688928.1:c.78G>A | ENSP00000509273.1:p.Lys26= | |
| ENST00000689118.1:c.78G>A | ENSP00000510554.1:p.Lys26= | |
| ENST00000689300.1:c.78G>A | ENSP00000510639.1:p.Lys26= | |
| ENST00000689997.1:c.-380-21192G>A | ENSP00000510700.1:n.-380-21192G>A | |
| ENST00000691151.1:n.370G>A | ||
| ENST00000691369.1:c.78G>A | ENSP00000509754.1:p.Lys26= | |
| ENST00000691441.1:c.78G>A | ENSP00000509686.1:p.Lys26= | |
| ENST00000691903.1:c.78G>A | ENSP00000510314.1:p.Lys26= | |
| ENST00000692776.1:c.78G>A | ENSP00000508524.1:p.Lys26= | |
| ENST00000369452.9:c.78G>A MANE Select | ENSP00000358464.5:p.Lys26= | |
| ENST00000265277.9:c.78G>A | ENSP00000265277.5:p.Lys26= | |
| ENST00000369452.8:c.78G>A | ENSP00000358464.4:p.Lys26= | |
| ENST00000480155.1:n.562G>A | ||
| ENST00000489390.1:n.56-35979G>A | ||
| ENST00000489783.1:n.456G>A | ||
| NM_001269039.1:c.78G>A | NP_001255968.1:p.Lys26= | |
| NM_007373.3:c.78G>A , LRG_753t1:c.78G>A | NP_031399.2:p.Lys26= | |
| XM_011540216.1:c.-380-21192G>A | XP_011538518.1:n.-380-21192G>A | |
| NM_001269039.2:c.78G>A | NP_001255968.1:p.Lys26= | |
| NM_001324336.1:c.78G>A | NP_001311265.1:p.Lys26= | |
| NM_001324337.1:c.78G>A | NP_001311266.1:p.Lys26= | |
| NR_136749.1:n.116-21192G>A | ||
| NM_007373.4:c.78G>A MANE Select | NP_031399.2:p.Lys26= | |
| NM_001269039.3:c.78G>A | NP_001255968.1:p.Lys26= | |
| NM_001324336.2:c.78G>A | NP_001311265.1:p.Lys26= | |
| NM_001324337.2:c.78G>A | NP_001311266.1:p.Lys26= | |
| NR_136749.2:n.55-21192G>A |