Canonical Allele Identifier: CA366894557
Gene: AHR HGNC NCBI

Linked Data

dbSNP Id: rs1407777824
gnomAD v2: 7-17379043-C-A
gnomAD v3: 7-17339419-C-A
gnomAD v4: 7-17339419-C-A

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.17339419C>A , CM000669.2:g.17339419C>A GRCh38
NC_000007.13:g.17379043C>A , CM000669.1:g.17379043C>A GRCh37
NC_000007.12:g.17345568C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000242057.9:c.1594C>A MANE Select ENSP00000242057.4:p.Gln532Lys
ENST00000637807.1:c.1564C>A ENSP00000490530.1:p.Gln522Lys
ENST00000642825.1:c.1549C>A ENSP00000495987.1:p.Gln517Lys
ENST00000242057.8:c.1594C>A ENSP00000242057.4:p.Gln532Lys
ENST00000463496.1:c.1594C>A ENSP00000436466.1:p.Gln532Lys
ENST00000492120.1:n.576C>A
NM_001621.4:c.1594C>A NP_001612.1:p.Gln532Lys
NM_001621.5:c.1594C>A MANE Select NP_001612.1:p.Gln532Lys