Canonical Allele Identifier: CA1141907830
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.172741810C= , CM000663.2:g.172741810C= GRCh38
NC_000001.10:g.172710950C= , CM000663.1:g.172710950C= GRCh37
NC_000001.9:g.170977573C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_922289.1:n.27-34009C=