Canonical Allele Identifier: CA1689218262
Gene:

Linked Data

dbSNP Id: rs1198916168

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.13400686G>A , CM000669.2:g.13400686G>A GRCh38
NC_000007.13:g.13440311G>A , CM000669.1:g.13440311G>A GRCh37
NC_000007.12:g.13406836G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001745097.1:n.147+90363G>A