Canonical Allele Identifier: CA1118845342
Gene:

Linked Data

dbSNP Id: rs140473930

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.125478688C>A , CM000670.2:g.125478688C>A GRCh38
NC_000008.10:g.126490930C>A , CM000670.1:g.126490930C>A GRCh37
NC_000008.9:g.126560112C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_928628.1:n.256+5374C>A