Canonical Allele Identifier: CA366895749
Gene: AHR HGNC NCBI

Linked Data

MyVariant Identifiers: chr7:g.17379474T>A (hg19) chr7:g.17339850T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.17339850T>A , CM000669.2:g.17339850T>A GRCh38
NC_000007.13:g.17379474T>A , CM000669.1:g.17379474T>A GRCh37
NC_000007.12:g.17345999T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000242057.9:c.2025T>A MANE Select ENSP00000242057.4:p.Phe675Leu
ENST00000637807.1:c.1995T>A ENSP00000490530.1:p.Phe665Leu
ENST00000642825.1:c.1980T>A ENSP00000495987.1:p.Phe660Leu
ENST00000242057.8:c.2025T>A ENSP00000242057.4:p.Phe675Leu
ENST00000463496.1:c.2025T>A ENSP00000436466.1:p.Phe675Leu
NM_001621.4:c.2025T>A NP_001612.1:p.Phe675Leu
NM_001621.5:c.2025T>A MANE Select NP_001612.1:p.Phe675Leu
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