Canonical Allele Identifier: CA1695606391
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.25831430T= , CM000669.2:g.25831430T= GRCh38
NC_000007.13:g.25871050T= , CM000669.1:g.25871050T= GRCh37
NC_000007.12:g.25837575T= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_108752.3:n.477A=
XR_927108.1:n.451A=
XR_927109.1:n.533A=
XR_927110.1:n.437A=
XR_108752.4:n.491A=
XR_927110.2:n.616A=