Canonical Allele Identifier: CA1691298730
Gene: AHR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.17293227T= , CM000669.2:g.17293227T= GRCh38
NC_000007.13:g.17332851T= , CM000669.1:g.17332851T= GRCh37
NC_000007.12:g.17299376T= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000642825.1:c.-202-3070T= ENSP00000495987.1:n.-202-3070T=
XR_927069.1:n.293+1939A=
XR_927070.1:n.293+1939A=
XR_927071.1:n.293+1939A=
XR_927072.1:n.294+1939A=
XR_927073.1:n.296-1856A=
XR_927073.2:n.296-1856A=