Canonical Allele Identifier: CA1580179020
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.126002701C= , CM000667.2:g.126002701C= GRCh38
NC_000005.9:g.125338394C= , CM000667.1:g.125338394C= GRCh37
NC_000005.8:g.125366293C= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_948737.1:n.565+3639G=
XR_948738.1:n.497+5839G=