Canonical Allele Identifier: CA366894579
Gene: AHR HGNC NCBI

Linked Data

dbSNP Id: rs1782393220

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.17339423A>G , CM000669.2:g.17339423A>G GRCh38
NC_000007.13:g.17379047A>G , CM000669.1:g.17379047A>G GRCh37
NC_000007.12:g.17345572A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000242057.9:c.1598A>G MANE Select ENSP00000242057.4:p.Asp533Gly
ENST00000637807.1:c.1568A>G ENSP00000490530.1:p.Asp523Gly
ENST00000642825.1:c.1553A>G ENSP00000495987.1:p.Asp518Gly
ENST00000242057.8:c.1598A>G ENSP00000242057.4:p.Asp533Gly
ENST00000463496.1:c.1598A>G ENSP00000436466.1:p.Asp533Gly
ENST00000492120.1:n.580A>G
NM_001621.4:c.1598A>G NP_001612.1:p.Asp533Gly
NM_001621.5:c.1598A>G MANE Select NP_001612.1:p.Asp533Gly