Canonical Allele Identifier: CA366895667
Gene: AHR HGNC NCBI

Linked Data

ClinVar Variation Id: 2046520
ClinVar RCV Id: RCV002886659
dbSNP Id: rs1393549175
gnomAD v2: 7-17379440-G-A
gnomAD v4: 7-17339816-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.17339816G>A , CM000669.2:g.17339816G>A GRCh38
NC_000007.13:g.17379440G>A , CM000669.1:g.17379440G>A GRCh37
NC_000007.12:g.17345965G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000242057.9:c.1991G>A MANE Select ENSP00000242057.4:p.Cys664Tyr
ENST00000637807.1:c.1961G>A ENSP00000490530.1:p.Cys654Tyr
ENST00000642825.1:c.1946G>A ENSP00000495987.1:p.Cys649Tyr
ENST00000242057.8:c.1991G>A ENSP00000242057.4:p.Cys664Tyr
ENST00000463496.1:c.1991G>A ENSP00000436466.1:p.Cys664Tyr
NM_001621.4:c.1991G>A NP_001612.1:p.Cys664Tyr
NM_001621.5:c.1991G>A MANE Select NP_001612.1:p.Cys664Tyr