Canonical Allele Identifier: CA11358693
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.41043968G>A , CM000665.2:g.41043968G>A GRCh38
NC_000003.11:g.41085459G>A , CM000665.1:g.41085459G>A GRCh37
NC_000003.10:g.41060463G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_940768.1:n.6C>T