Canonical Allele Identifier: CA2193710621
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.87419478C= , CM000677.2:g.87419478C= GRCh38
NC_000015.9:g.87962709C= , CM000677.1:g.87962709C= GRCh37
NC_000015.8:g.85763713C= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_932584.1:n.340-207G=
XR_932585.1:n.340-207G=
XR_001751647.1:n.617-207G=
XR_932585.2:n.627-207G=