Canonical Allele Identifier: CA1563552168
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.92222952A= , CM000667.2:g.92222952A= GRCh38
NC_000005.9:g.91518769A= , CM000667.1:g.91518769A= GRCh37
NC_000005.8:g.91554525A= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_948565.1:n.394+18268A=