Canonical Allele Identifier: CA4172220
Gene: AHR HGNC NCBI

Linked Data

ClinVar Variation Id: 1470663
ClinVar RCV Id: RCV001964291
dbSNP Id: rs765874987
gnomAD v2: 7-17379467-A-G
gnomAD v4: 7-17339843-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.17339843A>G , CM000669.2:g.17339843A>G GRCh38
NC_000007.13:g.17379467A>G , CM000669.1:g.17379467A>G GRCh37
NC_000007.12:g.17345992A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000242057.9:c.2018A>G MANE Select ENSP00000242057.4:p.Asn673Ser
ENST00000637807.1:c.1988A>G ENSP00000490530.1:p.Asn663Ser
ENST00000642825.1:c.1973A>G ENSP00000495987.1:p.Asn658Ser
ENST00000242057.8:c.2018A>G ENSP00000242057.4:p.Asn673Ser
ENST00000463496.1:c.2018A>G ENSP00000436466.1:p.Asn673Ser
NM_001621.4:c.2018A>G NP_001612.1:p.Asn673Ser
NM_001621.5:c.2018A>G MANE Select NP_001612.1:p.Asn673Ser