Canonical Allele Identifier:
CA2104925782
Gene:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000013.11:g.80049267G= , CM000675.2:g.80049267G= | GRCh38 |
| NC_000013.10:g.80623402G= , CM000675.1:g.80623402G= | GRCh37 |
| NC_000013.9:g.79521403G= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_245449.3:n.131+993C= | ||
| XR_942114.1:n.146+695C= |