Canonical Allele Identifier: CA1715429925
Gene:

Linked Data

dbSNP Id: rs1788209828

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.69147080G>A , CM000669.2:g.69147080G>A GRCh38
NC_000007.13:g.68612067G>A , CM000669.1:g.68612067G>A GRCh37
NC_000007.12:g.68250003G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_927647.1:n.88-954C>T