Canonical Allele Identifier: CA1462694135
Gene:

Linked Data

dbSNP Id: rs1678906180

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.62557947T>A , CM000666.2:g.62557947T>A GRCh38
NC_000004.11:g.63423665T>A , CM000666.1:g.63423665T>A GRCh37
NC_000004.10:g.63106260T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_938814.1:n.161-5897T>A