Canonical Allele Identifier: CA1691291728
Gene: AHR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.17285430G= , CM000669.2:g.17285430G= GRCh38
NC_000007.13:g.17325054G= , CM000669.1:g.17325054G= GRCh37
NC_000007.12:g.17291579G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000642825.1:c.-202-10867G= ENSP00000495987.1:n.-202-10867G=
XR_927069.1:n.567+813C=
XR_927070.1:n.567+813C=
XR_927071.1:n.567+813C=
XR_927072.1:n.568+813C=
XR_927073.2:n.711+813C=