Linked Data
ClinVar Variation Id:
663774
ClinVar RCV Id:
RCV000821724
dbSNP Id:
rs373613096
ExAC:
17:80037402 C / T
gnomAD v2:
17-80037402-C-T
gnomAD v3:
17-82079526-C-T
gnomAD v4:
17-82079526-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.82079526C>T , CM000679.2:g.82079526C>T | GRCh38 |
| NC_000017.10:g.80037402C>T , CM000679.1:g.80037402C>T | GRCh37 |
| NC_000017.9:g.77630691C>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000306749.4:c.7229G>A MANE Select | ENSP00000304592.2:p.Gly2410Asp | |
| ENST00000306749.3:c.7229G>A | ENSP00000304592.2:p.Gly2410Asp | |
| ENST00000578424.2:n.508G>A | ||
| ENST00000580382.1:c.399G>A | ||
| ENST00000584610.2:n.404G>A | ||
| ENST00000634990.1:c.7223G>A | ENSP00000488964.1:p.Gly2408Asp | |
| NM_004104.4:c.7229G>A | NP_004095.4:p.Gly2410Asp | |
| XM_011523538.1:c.7229G>A | XP_011521840.1:p.Gly2410Asp | |
| XM_011523538.2:c.7229G>A | XP_011521840.1:p.Gly2410Asp | |
| NM_004104.5:c.7229G>A MANE Select | NP_004095.4:p.Gly2410Asp |