Canonical Allele Identifier: CA366895651
Gene: AHR HGNC NCBI

Linked Data

dbSNP Id: rs1444974051
MyVariant Identifiers: chr7:g.17379433T>A (hg19) chr7:g.17339809T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.17339809T>A , CM000669.2:g.17339809T>A GRCh38
NC_000007.13:g.17379433T>A , CM000669.1:g.17379433T>A GRCh37
NC_000007.12:g.17345958T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000242057.9:c.1984T>A MANE Select ENSP00000242057.4:p.Phe662Ile
ENST00000637807.1:c.1954T>A ENSP00000490530.1:p.Phe652Ile
ENST00000642825.1:c.1939T>A ENSP00000495987.1:p.Phe647Ile
ENST00000242057.8:c.1984T>A ENSP00000242057.4:p.Phe662Ile
ENST00000463496.1:c.1984T>A ENSP00000436466.1:p.Phe662Ile
NM_001621.4:c.1984T>A NP_001612.1:p.Phe662Ile
NM_001621.5:c.1984T>A MANE Select NP_001612.1:p.Phe662Ile
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