Canonical Allele Identifier: CA4172193
Gene: AHR HGNC NCBI

Linked Data

ClinVar Variation Id: 1951803
ClinVar RCV Id: RCV002676499
dbSNP Id: rs775243780
ExAC: 7:17379302 A / G
gnomAD v2: 7-17379302-A-G
gnomAD v4: 7-17339678-A-G
MyVariant Identifiers: chr7:g.17379302A>G (hg19) chr7:g.17339678A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.17339678A>G , CM000669.2:g.17339678A>G GRCh38
NC_000007.13:g.17379302A>G , CM000669.1:g.17379302A>G GRCh37
NC_000007.12:g.17345827A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000242057.9:c.1853A>G MANE Select ENSP00000242057.4:p.His618Arg
ENST00000637807.1:c.1823A>G ENSP00000490530.1:p.His608Arg
ENST00000642825.1:c.1808A>G ENSP00000495987.1:p.His603Arg
ENST00000242057.8:c.1853A>G ENSP00000242057.4:p.His618Arg
ENST00000463496.1:c.1853A>G ENSP00000436466.1:p.His618Arg
NM_001621.4:c.1853A>G NP_001612.1:p.His618Arg
NM_001621.5:c.1853A>G MANE Select NP_001612.1:p.His618Arg
Search 100 bp 5'
Search 100 bp 3'