Canonical Allele Identifier: CA2715424659
Gene:

Linked Data

dbSNP Id: rs2116132115

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.97388361G>A , CM000669.2:g.97388361G>A GRCh38
NC_000007.13:g.97017673G>A , CM000669.1:g.97017673G>A GRCh37
NC_000007.12:g.96855609G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_001745293.1:n.127-59714C>T