Linked Data
dbSNP Id:
rs1819382351
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.21140495T>G , CM000671.2:g.21140495T>G | GRCh38 |
| NC_000009.11:g.21140494T>G , CM000671.1:g.21140494T>G | GRCh37 |
| NC_000009.10:g.21130494T>G | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000380229.3:c.*488A>C | ENSP00000369578.2:n.*488A>C |