Canonical Allele Identifier: CA1691298862
Gene: AHR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.17293378G= , CM000669.2:g.17293378G= GRCh38
NC_000007.13:g.17333002G= , CM000669.1:g.17333002G= GRCh37
NC_000007.12:g.17299527G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000642825.1:c.-202-2919G= ENSP00000495987.1:n.-202-2919G=
XR_927069.1:n.293+1788C=
XR_927070.1:n.293+1788C=
XR_927071.1:n.293+1788C=
XR_927072.1:n.294+1788C=
XR_927073.1:n.295+1788C=
XR_927073.2:n.295+1788C=