Canonical Allele Identifier: CA366895700
Gene: AHR HGNC NCBI

Linked Data

ClinVar Variation Id: 958185
ClinVar RCV Id: RCV001231302
dbSNP Id: rs1318083010
gnomAD v2: 7-17379453-C-G
gnomAD v4: 7-17339829-C-G
MyVariant Identifiers: chr7:g.17379453C>G (hg19) chr7:g.17339829C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.17339829C>G , CM000669.2:g.17339829C>G GRCh38
NC_000007.13:g.17379453C>G , CM000669.1:g.17379453C>G GRCh37
NC_000007.12:g.17345978C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000242057.9:c.2004C>G MANE Select ENSP00000242057.4:p.Asp668Glu
ENST00000637807.1:c.1974C>G ENSP00000490530.1:p.Asp658Glu
ENST00000642825.1:c.1959C>G ENSP00000495987.1:p.Asp653Glu
ENST00000242057.8:c.2004C>G ENSP00000242057.4:p.Asp668Glu
ENST00000463496.1:c.2004C>G ENSP00000436466.1:p.Asp668Glu
NM_001621.4:c.2004C>G NP_001612.1:p.Asp668Glu
NM_001621.5:c.2004C>G MANE Select NP_001612.1:p.Asp668Glu
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