Canonical Allele Identifier: CA797158428
Gene:

Linked Data

dbSNP Id: rs1392535027

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.62557841G>A , CM000666.2:g.62557841G>A GRCh38
NC_000004.11:g.63423559G>A , CM000666.1:g.63423559G>A GRCh37
NC_000004.10:g.63106154G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_938814.1:n.161-6003G>A