Canonical Allele Identifier: CA366895697
Gene: AHR HGNC NCBI

Linked Data

MyVariant Identifiers: chr7:g.17379452A>G (hg19) chr7:g.17339828A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.17339828A>G , CM000669.2:g.17339828A>G GRCh38
NC_000007.13:g.17379452A>G , CM000669.1:g.17379452A>G GRCh37
NC_000007.12:g.17345977A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000242057.9:c.2003A>G MANE Select ENSP00000242057.4:p.Asp668Gly
ENST00000637807.1:c.1973A>G ENSP00000490530.1:p.Asp658Gly
ENST00000642825.1:c.1958A>G ENSP00000495987.1:p.Asp653Gly
ENST00000242057.8:c.2003A>G ENSP00000242057.4:p.Asp668Gly
ENST00000463496.1:c.2003A>G ENSP00000436466.1:p.Asp668Gly
NM_001621.4:c.2003A>G NP_001612.1:p.Asp668Gly
NM_001621.5:c.2003A>G MANE Select NP_001612.1:p.Asp668Gly
Search 100 bp 5'
Search 100 bp 3'