Canonical Allele Identifier: CA366895650
Gene: AHR HGNC NCBI

Linked Data

MyVariant Identifiers: chr7:g.17379433T>C (hg19) chr7:g.17339809T>C (hg38)
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Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid Change
ENST00000242057.9:c.1984T>C MANE Select ENSP00000242057.4:p.Phe662Leu
ENST00000637807.1:c.1954T>C ENSP00000490530.1:p.Phe652Leu
ENST00000642825.1:c.1939T>C ENSP00000495987.1:p.Phe647Leu
ENST00000242057.8:c.1984T>C ENSP00000242057.4:p.Phe662Leu
ENST00000463496.1:c.1984T>C ENSP00000436466.1:p.Phe662Leu
NM_001621.4:c.1984T>C NP_001612.1:p.Phe662Leu
NM_001621.5:c.1984T>C MANE Select NP_001612.1:p.Phe662Leu
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