Canonical Allele Identifier: CA1207463788
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.172741897C= , CM000663.2:g.172741897C= GRCh38
NC_000001.10:g.172711037C= , CM000663.1:g.172711037C= GRCh37
NC_000001.9:g.170977660C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_922289.1:n.27-33922C=