Canonical Allele Identifier: CA454134218
Gene: AHR HGNC NCBI

Linked Data

ClinVar Variation Id: 2133739
ClinVar RCV Id: RCV003056368
gnomAD v4: 7-17339697-A-G
MyVariant Identifiers: chr7:g.17379321A>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.17339697A>G , CM000669.2:g.17339697A>G GRCh38
NC_000007.13:g.17379321A>G , CM000669.1:g.17379321A>G GRCh37
NC_000007.12:g.17345846A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000242057.9:c.1872A>G MANE Select ENSP00000242057.4:p.Gln624=
ENST00000637807.1:c.1842A>G ENSP00000490530.1:p.Gln614=
ENST00000642825.1:c.1827A>G ENSP00000495987.1:p.Gln609=
ENST00000242057.8:c.1872A>G ENSP00000242057.4:p.Gln624=
ENST00000463496.1:c.1872A>G ENSP00000436466.1:p.Gln624=
NM_001621.4:c.1872A>G NP_001612.1:p.Gln624=
NM_001621.5:c.1872A>G MANE Select NP_001612.1:p.Gln624=
Search 100 bp 5'
Search 100 bp 3'