Canonical Allele Identifier: CA1691290795
Gene: AHR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.17269572C= , CM000669.2:g.17269572C= GRCh38
NC_000007.13:g.17309196C= , CM000669.1:g.17309196C= GRCh37
NC_000007.12:g.17275721C= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000642825.1:c.-203+21846C= ENSP00000495987.1:n.-203+21846C=
XR_927073.2:n.785-10244G=