Canonical Allele Identifier: CA4172217
Gene: AHR HGNC NCBI

Linked Data

ClinVar Variation Id: 1405802
ClinVar RCV Id: RCV001906715
dbSNP Id: rs149039873
gnomAD v2: 7-17379445-C-A
gnomAD v3: 7-17339821-C-A
gnomAD v4: 7-17339821-C-A

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.17339821C>A , CM000669.2:g.17339821C>A GRCh38
NC_000007.13:g.17379445C>A , CM000669.1:g.17379445C>A GRCh37
NC_000007.12:g.17345970C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000242057.9:c.1996C>A MANE Select ENSP00000242057.4:p.Gln666Lys
ENST00000637807.1:c.1966C>A ENSP00000490530.1:p.Gln656Lys
ENST00000642825.1:c.1951C>A ENSP00000495987.1:p.Gln651Lys
ENST00000242057.8:c.1996C>A ENSP00000242057.4:p.Gln666Lys
ENST00000463496.1:c.1996C>A ENSP00000436466.1:p.Gln666Lys
NM_001621.4:c.1996C>A NP_001612.1:p.Gln666Lys
NM_001621.5:c.1996C>A MANE Select NP_001612.1:p.Gln666Lys