Linked Data
dbSNP Id:
rs1334918054
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.214088017A>T , CM000663.2:g.214088017A>T | GRCh38 |
| NC_000001.10:g.214261360A>T , CM000663.1:g.214261360A>T | GRCh37 |
| NC_000001.9:g.212327983A>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XM_011510303.1:c.-188-15579T>A | XP_011508605.1:n.-188-15579T>A | |
| XR_922584.1:n.119-15579T>A | ||
| XR_922584.2:n.261-15579T>A |