Canonical Allele Identifier: CA2756725788
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.70577227A>T , CM000665.2:g.70577227A>T GRCh38
NC_000003.11:g.70626378A>T , CM000665.1:g.70626378A>T GRCh37
NC_000003.10:g.70709068A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_940947.1:n.407-1274T>A
XR_001740559.1:n.367-1274T>A