Canonical Allele Identifier: CA1318169372
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.195006922A= , CM000664.2:g.195006922A= GRCh38
NC_000002.11:g.195871646A= , CM000664.1:g.195871646A= GRCh37
NC_000002.10:g.195579891A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001739836.1:n.553+52513T=