Canonical Allele Identifier: CA1691323964
Gene: AHR HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.17339787G= , CM000669.2:g.17339787G= GRCh38
NC_000007.13:g.17379411G= , CM000669.1:g.17379411G= GRCh37
NC_000007.12:g.17345936G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000242057.9:c.1962G= MANE Select ENSP00000242057.4:p.Trp654=
ENST00000637807.1:c.1932G= ENSP00000490530.1:p.Trp644=
ENST00000642825.1:c.1917G= ENSP00000495987.1:p.Trp639=
ENST00000242057.8:c.1962G= ENSP00000242057.4:p.Trp654=
ENST00000463496.1:c.1962G= ENSP00000436466.1:p.Trp654=
NM_001621.4:c.1962G= NP_001612.1:p.Trp654=
NM_001621.5:c.1962G= MANE Select NP_001612.1:p.Trp654=
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