Linked Data
ClinVar Variation Id:
2919815
ClinVar RCV Id:
RCV003736044
dbSNP Id:
rs368050715
ExAC:
16:2367682 G / A
gnomAD v2:
16-2367682-G-A
gnomAD v3:
16-2317681-G-A
gnomAD v4:
16-2317681-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.2317681G>A , CM000678.2:g.2317681G>A | GRCh38 |
| NC_000016.9:g.2367682G>A , CM000678.1:g.2367682G>A | GRCh37 |
| NC_000016.8:g.2307683G>A | NCBI36 |
| NG_011790.1:g.28066C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000301732.10:c.957C>T MANE Select | ENSP00000301732.5:p.Ala319= | |
| ENST00000301732.9:c.957C>T | ENSP00000301732.5:p.Ala319= | |
| ENST00000382381.7:c.957C>T | ENSP00000371818.3:p.Ala319= | |
| ENST00000563623.5:n.1520C>T | ||
| NM_001089.2:c.957C>T | NP_001080.2:p.Ala319= | |
| NM_001089.3:c.957C>T MANE Select | NP_001080.2:p.Ala319= |