Canonical Allele Identifier: CA1769514527
Gene:

Linked Data

dbSNP Id: rs1228468536

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.20734917C>A , CM000670.2:g.20734917C>A GRCh38
NC_000008.10:g.20592428C>A , CM000670.1:g.20592428C>A GRCh37
NC_000008.9:g.20636708C>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_949569.3:n.72-55529C>A