Canonical Allele Identifier: CA1691290799
Gene: AHR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.17269582C= , CM000669.2:g.17269582C= GRCh38
NC_000007.13:g.17309206C= , CM000669.1:g.17309206C= GRCh37
NC_000007.12:g.17275731C= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000642825.1:c.-203+21856C= ENSP00000495987.1:n.-203+21856C=
XR_927073.2:n.785-10254G=