Canonical Allele Identifier: CA1691323981
Gene: AHR HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.17339829C= , CM000669.2:g.17339829C= GRCh38
NC_000007.13:g.17379453C= , CM000669.1:g.17379453C= GRCh37
NC_000007.12:g.17345978C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000242057.9:c.2004C= MANE Select ENSP00000242057.4:p.Asp668=
ENST00000637807.1:c.1974C= ENSP00000490530.1:p.Asp658=
ENST00000642825.1:c.1959C= ENSP00000495987.1:p.Asp653=
ENST00000242057.8:c.2004C= ENSP00000242057.4:p.Asp668=
ENST00000463496.1:c.2004C= ENSP00000436466.1:p.Asp668=
NM_001621.4:c.2004C= NP_001612.1:p.Asp668=
NM_001621.5:c.2004C= MANE Select NP_001612.1:p.Asp668=
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