Linked Data
ClinVar Variation Id:
15350
ClinVar RCV Id:
RCV000016596
dbSNP Id:
rs33976006
COSMIC:
COSM5763940
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.5226668C>T , CM000673.2:g.5226668C>T | GRCh38 |
| NC_000011.9:g.5247898C>T , CM000673.1:g.5247898C>T | GRCh37 |
| NC_000011.8:g.5204474C>T | NCBI36 |
| NG_000007.3:g.70948G>A | |
| NG_059281.1:g.5404G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000647020.1:c.224G>A | ENSP00000494175.1:p.Gly75Asp | |
| ENST00000335295.4:c.224G>A MANE Select | ENSP00000333994.3:p.Gly75Asp | |
| ENST00000380315.2:c.224G>A | ENSP00000369671.2:p.Gly75Asp | |
| ENST00000475226.1:n.156G>A | ||
| ENST00000485743.1:n.275G>A | ||
| ENST00000633227.1:c.*40G>A | ENSP00000488004.1:n.*40G>A | |
| NM_000518.4:c.224G>A | NP_000509.1:p.Gly75Asp | |
| NM_000518.5:c.224G>A MANE Select | NP_000509.1:p.Gly75Asp |