Canonical Allele Identifier: CA2386472683
Community Standard Title: NC_000021.9:g.32997453C=
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.32997453C= , CM000683.2:g.32997453C= GRCh38
NC_000021.8:g.34369761C= , CM000683.1:g.34369761C= GRCh37
NC_000021.7:g.33291631C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_937671.1:n.396-21931C=