Canonical Allele Identifier: CA1695606388
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.25831410T= , CM000669.2:g.25831410T= GRCh38
NC_000007.13:g.25871030T= , CM000669.1:g.25871030T= GRCh37
NC_000007.12:g.25837555T= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_108752.3:n.497A=
XR_927108.1:n.471A=
XR_927109.1:n.553A=
XR_927110.1:n.457A=
XR_108752.4:n.511A=
XR_927110.2:n.636A=