Canonical Allele Identifier: CA1563552098
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.92222820C= , CM000667.2:g.92222820C= GRCh38
NC_000005.9:g.91518637C= , CM000667.1:g.91518637C= GRCh37
NC_000005.8:g.91554393C= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_948565.1:n.394+18136C=