Canonical Allele Identifier: CA197853369
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.108126198G>A , CM000671.2:g.108126198G>A GRCh38
NC_000009.11:g.110888478G>A , CM000671.1:g.110888478G>A GRCh37
NC_000009.10:g.109928299G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_930239.1:n.461-72904C>T
XR_001746881.1:n.668-72904C>T
XR_001746882.1:n.668-72904C>T