Linked Data
ClinVar Variation Id:
910782
dbSNP Id:
rs372072732
gnomAD v2:
7-107350528-G-A
gnomAD v3:
7-107710083-G-A
gnomAD v4:
7-107710083-G-A
COSMIC:
COSM241635
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.107710083G>A , CM000669.2:g.107710083G>A | GRCh38 |
| NC_000007.13:g.107350528G>A , CM000669.1:g.107350528G>A | GRCh37 |
| NC_000007.12:g.107137764G>A | NCBI36 |
| NG_008489.1:g.54449G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000644269.2:c.2119G>A MANE Select | ENSP00000494017.1:p.Gly707Arg | |
| ENST00000644846.1:c.775G>A | ||
| ENST00000265715.7:c.2119G>A | ENSP00000265715.3:p.Gly707Arg | |
| ENST00000492030.2:n.377-72G>A | ||
| NM_000441.1:c.2119G>A | NP_000432.1:p.Gly707Arg | |
| XM_005250425.1:c.2119G>A | XP_005250482.1:p.Gly707Arg | |
| XM_005250425.2:c.2119G>A | XP_005250482.1:p.Gly707Arg | |
| XM_017012318.1:c.2041G>A | XP_016867807.1:p.Gly681Arg | |
| NM_000441.2:c.2119G>A MANE Select | NP_000432.1:p.Gly707Arg |