Canonical Allele Identifier: CA587286153
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.25551261T>A , CM000671.2:g.25551261T>A GRCh38
NC_000009.11:g.25551259T>A , CM000671.1:g.25551259T>A GRCh37
NC_000009.10:g.25541259T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_929525.1:n.50-689A>T
XR_929525.2:n.674-689A>T