Canonical Allele Identifier: CA1580179022
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.126002715G= , CM000667.2:g.126002715G= GRCh38
NC_000005.9:g.125338408G= , CM000667.1:g.125338408G= GRCh37
NC_000005.8:g.125366307G= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_948737.1:n.565+3625C=
XR_948738.1:n.497+5825C=