Canonical Allele Identifier: CA1580179111
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.126002912T= , CM000667.2:g.126002912T= GRCh38
NC_000005.9:g.125338605T= , CM000667.1:g.125338605T= GRCh37
NC_000005.8:g.125366504T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_948737.1:n.565+3428A=
XR_948738.1:n.497+5628A=