Linked Data
ClinVar Variation Id:
1686765
ClinVar RCV Id:
RCV002248272
dbSNP Id:
rs140482278
ExAC:
9:75309630 C / A
gnomAD v2:
9-75309630-C-A
gnomAD v3:
9-72694714-C-A
gnomAD v4:
9-72694714-C-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.72694714C>A , CM000671.2:g.72694714C>A | GRCh38 |
| NC_000009.11:g.75309630C>A , CM000671.1:g.75309630C>A | GRCh37 |
| NC_000009.10:g.74499450C>A | NCBI36 |
| NG_008213.1:g.177914C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000297784.10:c.236C>A MANE Select | ENSP00000297784.6:p.Ala79Glu | |
| ENST00000644967.1:c.-77C>A | ENSP00000496159.1:n.-77C>A | |
| ENST00000645053.1:c.-77C>A | ENSP00000493838.1:n.-77C>A | |
| ENST00000645208.2:c.236C>A | ENSP00000494684.1:p.Ala79Glu | |
| ENST00000645773.1:c.236C>A | ENSP00000493698.1:p.Ala79Glu | |
| ENST00000645787.1:n.276C>A | ||
| ENST00000646244.1:n.686C>A | ||
| ENST00000646619.1:c.-77C>A | ENSP00000493726.1:n.-77C>A | |
| ENST00000650689.1:n.660C>A | ||
| ENST00000651183.1:c.-77C>A | ENSP00000498723.1:n.-77C>A | |
| ENST00000297784.9:c.236C>A | ENSP00000297784.5:p.Ala79Glu | |
| ENST00000340019.4:c.236C>A | ENSP00000341433.3:p.Ala79Glu | |
| NM_138691.2:c.236C>A | NP_619636.2:p.Ala79Glu | |
| XM_011518213.1:c.824C>A | XP_011516515.1:p.Ala275Glu | |
| XM_017014256.1:c.239C>A | XP_016869745.1:p.Ala80Glu | |
| NM_138691.3:c.236C>A MANE Select | NP_619636.2:p.Ala79Glu |