Canonical Allele Identifier: CA4172184
Gene: AHR HGNC NCBI

Linked Data

ClinVar Variation Id: 859723
ClinVar RCV Id: RCV001065897
dbSNP Id: rs374810935
gnomAD v2: 7-17379245-A-G
gnomAD v3: 7-17339621-A-G
gnomAD v4: 7-17339621-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.17339621A>G , CM000669.2:g.17339621A>G GRCh38
NC_000007.13:g.17379245A>G , CM000669.1:g.17379245A>G GRCh37
NC_000007.12:g.17345770A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000242057.9:c.1796A>G MANE Select ENSP00000242057.4:p.Tyr599Cys
ENST00000637807.1:c.1766A>G ENSP00000490530.1:p.Tyr589Cys
ENST00000642825.1:c.1751A>G ENSP00000495987.1:p.Tyr584Cys
ENST00000242057.8:c.1796A>G ENSP00000242057.4:p.Tyr599Cys
ENST00000463496.1:c.1796A>G ENSP00000436466.1:p.Tyr599Cys
NM_001621.4:c.1796A>G NP_001612.1:p.Tyr599Cys
NM_001621.5:c.1796A>G MANE Select NP_001612.1:p.Tyr599Cys