Canonical Allele Identifier: CA366895341
Gene: AHR HGNC NCBI

Linked Data

gnomAD v4: 7-17339679-T-A

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.17339679T>A , CM000669.2:g.17339679T>A GRCh38
NC_000007.13:g.17379303T>A , CM000669.1:g.17379303T>A GRCh37
NC_000007.12:g.17345828T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000242057.9:c.1854T>A MANE Select ENSP00000242057.4:p.His618Gln
ENST00000637807.1:c.1824T>A ENSP00000490530.1:p.His608Gln
ENST00000642825.1:c.1809T>A ENSP00000495987.1:p.His603Gln
ENST00000242057.8:c.1854T>A ENSP00000242057.4:p.His618Gln
ENST00000463496.1:c.1854T>A ENSP00000436466.1:p.His618Gln
NM_001621.4:c.1854T>A NP_001612.1:p.His618Gln
NM_001621.5:c.1854T>A MANE Select NP_001612.1:p.His618Gln