Canonical Allele Identifier: CA2756767567
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.72266810A>C , CM000665.2:g.72266810A>C GRCh38
NC_000003.11:g.72315961A>C , CM000665.1:g.72315961A>C GRCh37
NC_000003.10:g.72398651A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_940958.1:n.835+8298T>G