Canonical Allele Identifier: CA1691323955
Gene: AHR HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.17339760G= , CM000669.2:g.17339760G= GRCh38
NC_000007.13:g.17379384G= , CM000669.1:g.17379384G= GRCh37
NC_000007.12:g.17345909G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000242057.9:c.1935G= MANE Select ENSP00000242057.4:p.Met645=
ENST00000637807.1:c.1905G= ENSP00000490530.1:p.Met635=
ENST00000642825.1:c.1890G= ENSP00000495987.1:p.Met630=
ENST00000242057.8:c.1935G= ENSP00000242057.4:p.Met645=
ENST00000463496.1:c.1935G= ENSP00000436466.1:p.Met645=
NM_001621.4:c.1935G= NP_001612.1:p.Met645=
NM_001621.5:c.1935G= MANE Select NP_001612.1:p.Met645=
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