Canonical Allele Identifier: CA1462694138
Gene:

Linked Data

dbSNP Id: rs112567004

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.62557949G>A , CM000666.2:g.62557949G>A GRCh38
NC_000004.11:g.63423667G>A , CM000666.1:g.63423667G>A GRCh37
NC_000004.10:g.63106262G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_938814.1:n.161-5895G>A