Canonical Allele Identifier: CA1723810395
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.87913832T= , CM000669.2:g.87913832T= GRCh38
NC_000007.13:g.87543147T= , CM000669.1:g.87543147T= GRCh37
NC_000007.12:g.87381083T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_927723.1:n.148+69A=
XR_927724.1:n.192+69A=