Canonical Allele Identifier: CA1691323899
Gene: AHR HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.17339615C= , CM000669.2:g.17339615C= GRCh38
NC_000007.13:g.17379239C= , CM000669.1:g.17379239C= GRCh37
NC_000007.12:g.17345764C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000242057.9:c.1790C= MANE Select ENSP00000242057.4:p.Ser597=
ENST00000637807.1:c.1760C= ENSP00000490530.1:p.Ser587=
ENST00000642825.1:c.1745C= ENSP00000495987.1:p.Ser582=
ENST00000242057.8:c.1790C= ENSP00000242057.4:p.Ser597=
ENST00000463496.1:c.1790C= ENSP00000436466.1:p.Ser597=
NM_001621.4:c.1790C= NP_001612.1:p.Ser597=
NM_001621.5:c.1790C= MANE Select NP_001612.1:p.Ser597=
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