Canonical Allele Identifier: CA1691298878
Gene: AHR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.17293396A= , CM000669.2:g.17293396A= GRCh38
NC_000007.13:g.17333020A= , CM000669.1:g.17333020A= GRCh37
NC_000007.12:g.17299545A= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000642825.1:c.-202-2901A= ENSP00000495987.1:n.-202-2901A=
XR_927069.1:n.293+1770T=
XR_927070.1:n.293+1770T=
XR_927071.1:n.293+1770T=
XR_927072.1:n.294+1770T=
XR_927073.1:n.295+1770T=
XR_927073.2:n.295+1770T=