Canonical Allele Identifier: CA11357572
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.35101019G>T , CM000665.2:g.35101019G>T GRCh38
NC_000003.11:g.35142511G>T , CM000665.1:g.35142511G>T GRCh37
NC_000003.10:g.35117515G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_110817.1:n.206+205452C>A