Linked Data
ClinVar Variation Id:
225360
dbSNP Id:
rs761212672
ExAC:
1:152277475 G / T
gnomAD v2:
1-152277475-G-T
gnomAD v3:
1-152304999-G-T
gnomAD v4:
1-152304999-G-T
PubMed:
PMID:18200065
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.152304999G>T , CM000663.2:g.152304999G>T | GRCh38 |
| NC_000001.10:g.152277475G>T , CM000663.1:g.152277475G>T | GRCh37 |
| NC_000001.9:g.150544099G>T | NCBI36 |
| NG_016190.1:g.25205C>A , LRG_1028:g.25205C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000368799.2:c.9887C>A MANE Select | ENSP00000357789.1:p.Ser3296Ter | |
| ENST00000368799.1:c.9887C>A | ENSP00000357789.1:p.Ser3296Ter | |
| NM_002016.1:c.9887C>A , LRG_1028t1:c.9887C>A | NP_002007.1:p.Ser3296Ter | |
| XM_011509329.1:c.9108+779C>A | XP_011507631.1:n.9108+779C>A | |
| NM_002016.2:c.9887C>A MANE Select | NP_002007.1:p.Ser3296Ter |