Canonical Allele Identifier: CA1691323935
Gene: AHR HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.17339704C= , CM000669.2:g.17339704C= GRCh38
NC_000007.13:g.17379328C= , CM000669.1:g.17379328C= GRCh37
NC_000007.12:g.17345853C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000242057.9:c.1879C= MANE Select ENSP00000242057.4:p.Gln627=
ENST00000637807.1:c.1849C= ENSP00000490530.1:p.Gln617=
ENST00000642825.1:c.1834C= ENSP00000495987.1:p.Gln612=
ENST00000242057.8:c.1879C= ENSP00000242057.4:p.Gln627=
ENST00000463496.1:c.1879C= ENSP00000436466.1:p.Gln627=
NM_001621.4:c.1879C= NP_001612.1:p.Gln627=
NM_001621.5:c.1879C= MANE Select NP_001612.1:p.Gln627=
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