Canonical Allele Identifier: CA1258276543
Gene:

Linked Data

dbSNP Id: rs1672711736

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.67637526G>A , CM000664.2:g.67637526G>A GRCh38
NC_000002.11:g.67864658G>A , CM000664.1:g.67864658G>A GRCh37
NC_000002.10:g.67718162G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001739524.1:n.65+13440C>T