Linked Data
dbSNP Id:
rs983646222
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.21140585C>G , CM000671.2:g.21140585C>G | GRCh38 |
| NC_000009.11:g.21140584C>G , CM000671.1:g.21140584C>G | GRCh37 |
| NC_000009.10:g.21130584C>G | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000380229.3:c.*398G>C | ENSP00000369578.2:n.*398G>C |