Canonical Allele Identifier: CA2713951976
Gene: AHR HGNC NCBI

Linked Data

dbSNP Id: rs2115321928

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.17269583T>A , CM000669.2:g.17269583T>A GRCh38
NC_000007.13:g.17309207T>A , CM000669.1:g.17309207T>A GRCh37
NC_000007.12:g.17275732T>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000642825.1:c.-203+21857T>A ENSP00000495987.1:n.-203+21857T>A
XR_927073.2:n.785-10255A>T