Canonical Allele Identifier: CA1691255516
Gene: AHR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.17244893T= , CM000669.2:g.17244893T= GRCh38
NC_000007.13:g.17284517T= , CM000669.1:g.17284517T= GRCh37
NC_000007.12:g.17251042T= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000642825.1:c.-955-2081T= ENSP00000495987.1:n.-955-2081T=
XR_927073.2:n.861+14359A=