Canonical Allele Identifier: CA11610070
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.81952561G>T , CM000665.2:g.81952561G>T GRCh38
NC_000003.11:g.82001712G>T , CM000665.1:g.82001712G>T GRCh37
NC_000003.10:g.82084402G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_940999.1:n.463-559G>T
XR_940999.2:n.463-559G>T