Canonical Allele Identifier: CA366895525
Gene: AHR HGNC NCBI

Linked Data

dbSNP Id: rs1782398464

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.17339756A>G , CM000669.2:g.17339756A>G GRCh38
NC_000007.13:g.17379380A>G , CM000669.1:g.17379380A>G GRCh37
NC_000007.12:g.17345905A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000242057.9:c.1931A>G MANE Select ENSP00000242057.4:p.His644Arg
ENST00000637807.1:c.1901A>G ENSP00000490530.1:p.His634Arg
ENST00000642825.1:c.1886A>G ENSP00000495987.1:p.His629Arg
ENST00000242057.8:c.1931A>G ENSP00000242057.4:p.His644Arg
ENST00000463496.1:c.1931A>G ENSP00000436466.1:p.His644Arg
NM_001621.4:c.1931A>G NP_001612.1:p.His644Arg
NM_001621.5:c.1931A>G MANE Select NP_001612.1:p.His644Arg