Canonical Allele Identifier:
CA2751933701
Gene:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.120551739A>T , CM000664.2:g.120551739A>T | GRCh38 |
| NC_000002.11:g.121309315A>T , CM000664.1:g.121309315A>T | GRCh37 |
| NC_000002.10:g.121025785A>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_923262.1:n.1487+149T>A | ||
| XR_001739680.2:n.1495+149T>A | ||
| XR_001739681.2:n.2128+149T>A | ||
| XR_001739682.1:n.1495+149T>A | ||
| XR_002959417.1:n.1495+149T>A |