Canonical Allele Identifier: CA1691323989
Gene: AHR HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.17339852C= , CM000669.2:g.17339852C= GRCh38
NC_000007.13:g.17379476C= , CM000669.1:g.17379476C= GRCh37
NC_000007.12:g.17346001C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000242057.9:c.2027C= MANE Select ENSP00000242057.4:p.Thr676=
ENST00000637807.1:c.1997C= ENSP00000490530.1:p.Thr666=
ENST00000642825.1:c.1982C= ENSP00000495987.1:p.Thr661=
ENST00000242057.8:c.2027C= ENSP00000242057.4:p.Thr676=
ENST00000463496.1:c.2027C= ENSP00000436466.1:p.Thr676=
NM_001621.4:c.2027C= NP_001612.1:p.Thr676=
NM_001621.5:c.2027C= MANE Select NP_001612.1:p.Thr676=
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