Canonical Allele Identifier: CA1207463768
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.172741861T= , CM000663.2:g.172741861T= GRCh38
NC_000001.10:g.172711001T= , CM000663.1:g.172711001T= GRCh37
NC_000001.9:g.170977624T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_922289.1:n.27-33958T=