Canonical Allele Identifier: CA1691323982
Gene: AHR HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.17339835A= , CM000669.2:g.17339835A= GRCh38
NC_000007.13:g.17379459A= , CM000669.1:g.17379459A= GRCh37
NC_000007.12:g.17345984A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000242057.9:c.2010A= MANE Select ENSP00000242057.4:p.Gln670=
ENST00000637807.1:c.1980A= ENSP00000490530.1:p.Gln660=
ENST00000642825.1:c.1965A= ENSP00000495987.1:p.Gln655=
ENST00000242057.8:c.2010A= ENSP00000242057.4:p.Gln670=
ENST00000463496.1:c.2010A= ENSP00000436466.1:p.Gln670=
NM_001621.4:c.2010A= NP_001612.1:p.Gln670=
NM_001621.5:c.2010A= MANE Select NP_001612.1:p.Gln670=
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