Canonical Allele Identifier: CA1563552231
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.92223069C= , CM000667.2:g.92223069C= GRCh38
NC_000005.9:g.91518886C= , CM000667.1:g.91518886C= GRCh37
NC_000005.8:g.91554642C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_948565.1:n.394+18385C=