Canonical Allele Identifier: CA1841175486
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.25551271G>A , CM000671.2:g.25551271G>A GRCh38
NC_000009.11:g.25551269G>A , CM000671.1:g.25551269G>A GRCh37
NC_000009.10:g.25541269G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_929525.1:n.50-699C>T
XR_929525.2:n.674-699C>T