Canonical Allele Identifier:
CA15790465
Gene:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000013.11:g.34032049A>G , CM000675.2:g.34032049A>G | GRCh38 |
| NC_000013.10:g.34606186A>G , CM000675.1:g.34606186A>G | GRCh37 |
| NC_000013.9:g.33504186A>G | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_001749817.1:n.1515T>C |