Canonical Allele Identifier:
CA2700867575
Gene:
Linked Data
dbSNP Id:
rs2105325472
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.155870517T>A , CM000664.2:g.155870517T>A | GRCh38 |
| NC_000002.11:g.156727029T>A , CM000664.1:g.156727029T>A | GRCh37 |
| NC_000002.10:g.156435275T>A | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_923501.1:n.320-3330A>T | ||
| XR_001739749.1:n.331-29533A>T | ||
| XR_001739750.1:n.331-29533A>T | ||
| XR_001739751.1:n.331-29533A>T | ||
| XR_923501.2:n.331-3330A>T |