Canonical Allele Identifier: CA2510361529
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.25551503G>T , CM000671.2:g.25551503G>T GRCh38
NC_000009.11:g.25551501G>T , CM000671.1:g.25551501G>T GRCh37
NC_000009.10:g.25541501G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_929525.1:n.50-931C>A
XR_929525.2:n.674-931C>A