Canonical Allele Identifier: CA1462694309
Gene:

Linked Data

dbSNP Id: rs1756230066

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.62558293T>A , CM000666.2:g.62558293T>A GRCh38
NC_000004.11:g.63424011T>A , CM000666.1:g.63424011T>A GRCh37
NC_000004.10:g.63106606T>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_938814.1:n.161-5551T>A