Canonical Allele Identifier: CA1691299026
Gene: AHR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.17293554C= , CM000669.2:g.17293554C= GRCh38
NC_000007.13:g.17333178C= , CM000669.1:g.17333178C= GRCh37
NC_000007.12:g.17299703C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000642825.1:c.-202-2743C= ENSP00000495987.1:n.-202-2743C=
XR_927069.1:n.293+1612G=
XR_927070.1:n.293+1612G=
XR_927071.1:n.293+1612G=
XR_927072.1:n.294+1612G=
XR_927073.1:n.295+1612G=
XR_927073.2:n.295+1612G=