Canonical Allele Identifier: CA1695606389
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.25831423C= , CM000669.2:g.25831423C= GRCh38
NC_000007.13:g.25871043C= , CM000669.1:g.25871043C= GRCh37
NC_000007.12:g.25837568C= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_108752.3:n.484G=
XR_927108.1:n.458G=
XR_927109.1:n.540G=
XR_927110.1:n.444G=
XR_108752.4:n.498G=
XR_927110.2:n.623G=