Canonical Allele Identifier: CA4172218
Gene: AHR HGNC NCBI

Linked Data

ClinVar Variation Id: 1129663
ClinVar RCV Id: RCV001462880
dbSNP Id: rs772864138
ExAC: 7:17379459 A / G
gnomAD v2: 7-17379459-A-G
gnomAD v4: 7-17339835-A-G
MyVariant Identifiers: chr7:g.17379459A>G (hg19) chr7:g.17339835A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.17339835A>G , CM000669.2:g.17339835A>G GRCh38
NC_000007.13:g.17379459A>G , CM000669.1:g.17379459A>G GRCh37
NC_000007.12:g.17345984A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000242057.9:c.2010A>G MANE Select ENSP00000242057.4:p.Gln670=
ENST00000637807.1:c.1980A>G ENSP00000490530.1:p.Gln660=
ENST00000642825.1:c.1965A>G ENSP00000495987.1:p.Gln655=
ENST00000242057.8:c.2010A>G ENSP00000242057.4:p.Gln670=
ENST00000463496.1:c.2010A>G ENSP00000436466.1:p.Gln670=
NM_001621.4:c.2010A>G NP_001612.1:p.Gln670=
NM_001621.5:c.2010A>G MANE Select NP_001612.1:p.Gln670=
Search 100 bp 5'
Search 100 bp 3'