Canonical Allele Identifier: CA1691290805
Gene: AHR HGNC NCBI

Linked Data

dbSNP Id: rs970241707

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.17269585T>C , CM000669.2:g.17269585T>C GRCh38
NC_000007.13:g.17309209T>C , CM000669.1:g.17309209T>C GRCh37
NC_000007.12:g.17275734T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000642825.1:c.-203+21859T>C ENSP00000495987.1:n.-203+21859T>C
XR_927073.2:n.785-10257A>G