Canonical Allele Identifier:
CA2809140967
Gene:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.29376233A>T , CM000679.2:g.29376233A>T | GRCh38 |
| NC_000017.10:g.27703251A>T , CM000679.1:g.27703251A>T | GRCh37 |
| NC_000017.9:g.24727377A>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XM_011525588.1:c.1008-5928T>A | XP_011523890.1:n.1008-5928T>A |