Canonical Allele Identifier: CA4172216
Gene: AHR HGNC NCBI

Linked Data

ClinVar Variation Id: 1026100
ClinVar RCV Id: RCV001326505
dbSNP Id: rs114489761
ExAC: 7:17379437 A / C
gnomAD v2: 7-17379437-A-C
gnomAD v4: 7-17339813-A-C
MyVariant Identifiers: chr7:g.17379437A>C (hg19) chr7:g.17339813A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.17339813A>C , CM000669.2:g.17339813A>C GRCh38
NC_000007.13:g.17379437A>C , CM000669.1:g.17379437A>C GRCh37
NC_000007.12:g.17345962A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000242057.9:c.1988A>C MANE Select ENSP00000242057.4:p.Asn663Thr
ENST00000637807.1:c.1958A>C ENSP00000490530.1:p.Asn653Thr
ENST00000642825.1:c.1943A>C ENSP00000495987.1:p.Asn648Thr
ENST00000242057.8:c.1988A>C ENSP00000242057.4:p.Asn663Thr
ENST00000463496.1:c.1988A>C ENSP00000436466.1:p.Asn663Thr
NM_001621.4:c.1988A>C NP_001612.1:p.Asn663Thr
NM_001621.5:c.1988A>C MANE Select NP_001612.1:p.Asn663Thr
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