Canonical Allele Identifier: CA2756767577
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.72266826A>C , CM000665.2:g.72266826A>C GRCh38
NC_000003.11:g.72315977A>C , CM000665.1:g.72315977A>C GRCh37
NC_000003.10:g.72398667A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_940958.1:n.835+8282T>G