Canonical Allele Identifier: CA1968513085
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.45506632T= , CM000673.2:g.45506632T= GRCh38
NC_000011.9:g.45528182T= , CM000673.1:g.45528182T= GRCh37
NC_000011.8:g.45484758T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001748204.2:n.909-16861A=
XR_931245.3:n.566-16861A=