Canonical Allele Identifier: CA1690484151
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.15703161G= , CM000669.2:g.15703161G= GRCh38
NC_000007.13:g.15742786G= , CM000669.1:g.15742786G= GRCh37
NC_000007.12:g.15709311G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_927057.1:n.450+375G=
XR_001745101.1:n.704+375G=
XR_927057.2:n.704+375G=