Canonical Allele Identifier: CA1769514529
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.20734918G= , CM000670.2:g.20734918G= GRCh38
NC_000008.10:g.20592429G= , CM000670.1:g.20592429G= GRCh37
NC_000008.9:g.20636709G= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_949569.3:n.72-55528G=