Canonical Allele Identifier: CA154827754
Gene: AHR HGNC NCBI

Linked Data

dbSNP Id: rs866072193
gnomAD v2: 7-17333048-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.17293424G>A , CM000669.2:g.17293424G>A GRCh38
NC_000007.13:g.17333048G>A , CM000669.1:g.17333048G>A GRCh37
NC_000007.12:g.17299573G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000642825.1:c.-202-2873G>A ENSP00000495987.1:n.-202-2873G>A
XR_927069.1:n.293+1742C>T
XR_927070.1:n.293+1742C>T
XR_927071.1:n.293+1742C>T
XR_927072.1:n.294+1742C>T
XR_927073.1:n.295+1742C>T
XR_927073.2:n.295+1742C>T