Canonical Allele Identifier: CA1687324632
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.9816861T= , CM000669.2:g.9816861T= GRCh38
NC_000007.13:g.9856490T= , CM000669.1:g.9856490T= GRCh37
NC_000007.12:g.9823015T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_927024.1:n.209+49929A=
XR_927025.1:n.323+49929A=
XR_927026.1:n.209+49929A=
XR_927026.2:n.209+49929A=