Canonical Allele Identifier: CA1462694129
Gene:

Linked Data

dbSNP Id: rs1756225105

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.62557943C>A , CM000666.2:g.62557943C>A GRCh38
NC_000004.11:g.63423661C>A , CM000666.1:g.63423661C>A GRCh37
NC_000004.10:g.63106256C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_938814.1:n.161-5901C>A