Linked Data
dbSNP Id:
rs1281300485
gnomAD v3:
19-7527543-G-A
gnomAD v4:
19-7527543-G-A
COSMIC:
COSM1397562
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.7527543G>A , CM000681.2:g.7527543G>A | GRCh38 |
| NC_000019.9:g.7592429G>A , CM000681.1:g.7592429G>A | GRCh37 |
| NC_000019.8:g.7498429G>A | NCBI36 |
| NG_015806.1:g.9934G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000264079.11:c.595G>A MANE Select | ENSP00000264079.5:p.Glu199Lys | |
| ENST00000264079.10:c.595G>A | ENSP00000264079.5:p.Glu199Lys | |
| ENST00000394321.9:n.675G>A | ||
| ENST00000598406.1:n.416G>A | ||
| ENST00000601003.1:c.572-321G>A | ENSP00000469074.1:n.572-321G>A | |
| NM_020533.2:c.595G>A | NP_065394.1:p.Glu199Lys | |
| NM_020533.3:c.595G>A MANE Select | NP_065394.1:p.Glu199Lys |