Canonical Allele Identifier: CA1258276541
Gene:

Linked Data

dbSNP Id: rs1672711688

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.67637521C>G , CM000664.2:g.67637521C>G GRCh38
NC_000002.11:g.67864653C>G , CM000664.1:g.67864653C>G GRCh37
NC_000002.10:g.67718157C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001739524.1:n.65+13445G>C