Canonical Allele Identifier: CA1931617889
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.100101740T= , CM000672.2:g.100101740T= GRCh38
NC_000010.10:g.101861497T= , CM000672.1:g.101861497T= GRCh37
NC_000010.9:g.101851487T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_946245.1:n.185+5503T=