Canonical Allele Identifier: CA2578837761
Gene: AHR HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.17339859dup , CM000669.2:g.17339859dup GRCh38
NC_000007.13:g.17379483dup , CM000669.1:g.17379483dup GRCh37
NC_000007.12:g.17346008dup NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000242057.9:c.2034dup MANE Select ENSP00000242057.4:p.His679ThrfsTer12
ENST00000637807.1:c.2004dup ENSP00000490530.1:p.His669ThrfsTer12
ENST00000642825.1:c.1989dup ENSP00000495987.1:p.His664ThrfsTer12
ENST00000242057.8:c.2034dup ENSP00000242057.4:p.His679ThrfsTer12
ENST00000463496.1:c.2034dup ENSP00000436466.1:p.His679ThrfsTer12
NM_001621.4:c.2034dup NP_001612.1:p.His679ThrfsTer12
NM_001621.5:c.2034dup MANE Select NP_001612.1:p.His679ThrfsTer12
Search 100 bp 5'
Search 100 bp 3'