Canonical Allele Identifier: CA1563552089
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.92222804A= , CM000667.2:g.92222804A= GRCh38
NC_000005.9:g.91518621A= , CM000667.1:g.91518621A= GRCh37
NC_000005.8:g.91554377A= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_948565.1:n.394+18120A=