Canonical Allele Identifier: CA573128451
Gene: AHR HGNC NCBI

Linked Data

dbSNP Id: rs1157128032
gnomAD v2: 7-17309213-T-G

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.17269589T>G , CM000669.2:g.17269589T>G GRCh38
NC_000007.13:g.17309213T>G , CM000669.1:g.17309213T>G GRCh37
NC_000007.12:g.17275738T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000642825.1:c.-203+21863T>G ENSP00000495987.1:n.-203+21863T>G
XR_927073.2:n.785-10261A>C