Canonical Allele Identifier: CA366895698
Gene: AHR HGNC NCBI

Linked Data

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid Change
ENST00000242057.9:c.2003A>T MANE Select ENSP00000242057.4:p.Asp668Val
ENST00000637807.1:c.1973A>T ENSP00000490530.1:p.Asp658Val
ENST00000642825.1:c.1958A>T ENSP00000495987.1:p.Asp653Val
ENST00000242057.8:c.2003A>T ENSP00000242057.4:p.Asp668Val
ENST00000463496.1:c.2003A>T ENSP00000436466.1:p.Asp668Val
NM_001621.4:c.2003A>T NP_001612.1:p.Asp668Val
NM_001621.5:c.2003A>T MANE Select NP_001612.1:p.Asp668Val