Canonical Allele Identifier: CA366895769
Gene: AHR HGNC NCBI

Linked Data

MyVariant Identifiers: chr7:g.17379483A>T (hg19) chr7:g.17339859A>T (hg38)
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Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid Change
ENST00000242057.9:c.2034A>T MANE Select ENSP00000242057.4:p.Leu678Phe
ENST00000637807.1:c.2004A>T ENSP00000490530.1:p.Leu668Phe
ENST00000642825.1:c.1989A>T ENSP00000495987.1:p.Leu663Phe
ENST00000242057.8:c.2034A>T ENSP00000242057.4:p.Leu678Phe
ENST00000463496.1:c.2034A>T ENSP00000436466.1:p.Leu678Phe
NM_001621.4:c.2034A>T NP_001612.1:p.Leu678Phe
NM_001621.5:c.2034A>T MANE Select NP_001612.1:p.Leu678Phe
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