Canonical Allele Identifier: CA366895576
Gene: AHR HGNC NCBI

Linked Data

MyVariant Identifiers: chr7:g.17379401T>G (hg19) chr7:g.17339777T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.17339777T>G , CM000669.2:g.17339777T>G GRCh38
NC_000007.13:g.17379401T>G , CM000669.1:g.17379401T>G GRCh37
NC_000007.12:g.17345926T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000242057.9:c.1952T>G MANE Select ENSP00000242057.4:p.Phe651Cys
ENST00000637807.1:c.1922T>G ENSP00000490530.1:p.Phe641Cys
ENST00000642825.1:c.1907T>G ENSP00000495987.1:p.Phe636Cys
ENST00000242057.8:c.1952T>G ENSP00000242057.4:p.Phe651Cys
ENST00000463496.1:c.1952T>G ENSP00000436466.1:p.Phe651Cys
NM_001621.4:c.1952T>G NP_001612.1:p.Phe651Cys
NM_001621.5:c.1952T>G MANE Select NP_001612.1:p.Phe651Cys
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