Canonical Allele Identifier: CA1691255554
Gene: AHR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.17244937C= , CM000669.2:g.17244937C= GRCh38
NC_000007.13:g.17284561C= , CM000669.1:g.17284561C= GRCh37
NC_000007.12:g.17251086C= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000642825.1:c.-955-2037C= ENSP00000495987.1:n.-955-2037C=
XR_927073.2:n.861+14315G=