Canonical Allele Identifier: CA1563552162
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.92222941T= , CM000667.2:g.92222941T= GRCh38
NC_000005.9:g.91518758T= , CM000667.1:g.91518758T= GRCh37
NC_000005.8:g.91554514T= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_948565.1:n.394+18257T=