Canonical Allele Identifier: CA1723810367
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.87913763G= , CM000669.2:g.87913763G= GRCh38
NC_000007.13:g.87543078G= , CM000669.1:g.87543078G= GRCh37
NC_000007.12:g.87381014G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_927723.1:n.148+138C=
XR_927724.1:n.192+138C=