Canonical Allele Identifier: CA1691258407
Gene: AHR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.17247645A= , CM000669.2:g.17247645A= GRCh38
NC_000007.13:g.17287269A= , CM000669.1:g.17287269A= GRCh37
NC_000007.12:g.17253794A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000642825.1:c.-284A= ENSP00000495987.1:n.-284A=
XR_927073.2:n.861+11607T=