Canonical Allele Identifier: CA836199932
Gene: AHR HGNC NCBI

Linked Data

dbSNP Id: rs1448635323

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.17293251G>A , CM000669.2:g.17293251G>A GRCh38
NC_000007.13:g.17332875G>A , CM000669.1:g.17332875G>A GRCh37
NC_000007.12:g.17299400G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000642825.1:c.-202-3046G>A ENSP00000495987.1:n.-202-3046G>A
XR_927069.1:n.293+1915C>T
XR_927070.1:n.293+1915C>T
XR_927071.1:n.293+1915C>T
XR_927072.1:n.294+1915C>T
XR_927073.1:n.296-1880C>T
XR_927073.2:n.296-1880C>T