Linked Data
ClinVar Variation Id:
703129
ClinVar RCV Id:
RCV003103854
dbSNP Id:
rs202139687
ExAC:
2:121713000 G / A
gnomAD v2:
2-121713000-G-A
gnomAD v3:
2-120955424-G-A
gnomAD v4:
2-120955424-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.120955424G>A , CM000664.2:g.120955424G>A | GRCh38 |
| NC_000002.11:g.121713000G>A , CM000664.1:g.121713000G>A | GRCh37 |
| NC_000002.10:g.121429470G>A | NCBI36 |
| NG_009030.1:g.163134G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000361492.9:c.637G>A MANE Select | ENSP00000354586.5:p.Val213Met | |
| ENST00000452319.6:c.637G>A | ENSP00000390436.1:p.Val213Met | |
| ENST00000314490.15:c.-139-14969G>A | ENSP00000312694.12:n.-139-14969G>A | |
| ENST00000341310.10:c.149-14969G>A | ENSP00000344473.6:n.149-14969G>A | |
| ENST00000360874.10:c.231-13290G>A | ENSP00000441454.1:n.231-13290G>A | |
| ENST00000361492.8:c.637G>A | ENSP00000354586.4:p.Val213Met | |
| ENST00000433812.1:c.507G>A | ENSP00000402383.1:n.507G>A | |
| ENST00000435313.6:n.662G>A | ||
| ENST00000437950.5:c.149-14969G>A | ENSP00000415773.1:n.149-14969G>A | |
| ENST00000438299.5:c.149-14969G>A | ENSP00000400593.1:n.149-14969G>A | |
| ENST00000445186.5:c.149-14969G>A | ENSP00000397488.1:n.149-14969G>A | |
| ENST00000452319.5:c.637G>A | ENSP00000390436.1:p.Val213Met | |
| ENST00000452692.5:c.149-14969G>A | ENSP00000403715.1:n.149-14969G>A | |
| NM_005270.4:c.637G>A | NP_005261.2:p.Val213Met | |
| XM_006712422.1:c.637G>A | XP_006712485.1:p.Val213Met | |
| XM_011510969.1:c.619G>A | XP_011509271.1:p.Val207Met | |
| XM_011510970.1:c.496G>A | XP_011509272.1:p.Val166Met | |
| XM_011510971.1:c.442G>A | XP_011509273.1:p.Val148Met | |
| XM_011510972.1:c.442G>A | XP_011509274.1:p.Val148Met | |
| XM_011510973.1:c.262G>A | XP_011509275.1:p.Val88Met | |
| XM_011510974.1:c.262G>A | XP_011509276.1:p.Val88Met | |
| XM_006712422.3:c.637G>A | XP_006712485.1:p.Val213Met | |
| XM_011510969.2:c.889G>A | XP_011509271.2:p.Val297Met | |
| XM_011510970.2:c.496G>A | XP_011509272.1:p.Val166Met | |
| XM_011510971.2:c.442G>A | XP_011509273.1:p.Val148Met | |
| XM_011510972.2:c.538G>A | XP_011509274.2:p.Val180Met | |
| XM_011510973.2:c.262G>A | XP_011509275.1:p.Val88Met | |
| XM_011510974.2:c.262G>A | XP_011509276.1:p.Val88Met | |
| XM_017003818.1:c.889G>A | XP_016859307.1:p.Val297Met | |
| XM_024452794.1:c.637G>A | XP_024308562.1:p.Val213Met | |
| XM_024452795.1:c.637G>A | XP_024308563.1:p.Val213Met | |
| NM_001371271.1:c.637G>A | NP_001358200.1:p.Val213Met | |
| NM_001374353.1:c.637G>A MANE Select | NP_001361282.1:p.Val213Met | |
| NM_001374354.1:c.262G>A | NP_001361283.1:p.Val88Met | |
| NM_005270.5:c.637G>A | NP_005261.2:p.Val213Met |