Canonical Allele Identifier: CA1986002922
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.81143501T= , CM000673.2:g.81143501T= GRCh38
NC_000011.9:g.80854544T= , CM000673.1:g.80854544T= GRCh37
NC_000011.8:g.80532192T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_247272.2:n.46+109425A=