Canonical Allele Identifier: CA11457327
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.150324831G>A , CM000665.2:g.150324831G>A GRCh38
NC_000003.11:g.150042618G>A , CM000665.1:g.150042618G>A GRCh37
NC_000003.10:g.151525308G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001740958.1:n.1981+16432G>A