Canonical Allele Identifier: CA366895358
Gene: AHR HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.17339687A>G , CM000669.2:g.17339687A>G GRCh38
NC_000007.13:g.17379311A>G , CM000669.1:g.17379311A>G GRCh37
NC_000007.12:g.17345836A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000242057.9:c.1862A>G MANE Select ENSP00000242057.4:p.Gln621Arg
ENST00000637807.1:c.1832A>G ENSP00000490530.1:p.Gln611Arg
ENST00000642825.1:c.1817A>G ENSP00000495987.1:p.Gln606Arg
ENST00000242057.8:c.1862A>G ENSP00000242057.4:p.Gln621Arg
ENST00000463496.1:c.1862A>G ENSP00000436466.1:p.Gln621Arg
NM_001621.4:c.1862A>G NP_001612.1:p.Gln621Arg
NM_001621.5:c.1862A>G MANE Select NP_001612.1:p.Gln621Arg