Canonical Allele Identifier: CA366895383
Gene: AHR HGNC NCBI

Linked Data

gnomAD v4: 7-17339697-A-C

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.17339697A>C , CM000669.2:g.17339697A>C GRCh38
NC_000007.13:g.17379321A>C , CM000669.1:g.17379321A>C GRCh37
NC_000007.12:g.17345846A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000242057.9:c.1872A>C MANE Select ENSP00000242057.4:p.Gln624His
ENST00000637807.1:c.1842A>C ENSP00000490530.1:p.Gln614His
ENST00000642825.1:c.1827A>C ENSP00000495987.1:p.Gln609His
ENST00000242057.8:c.1872A>C ENSP00000242057.4:p.Gln624His
ENST00000463496.1:c.1872A>C ENSP00000436466.1:p.Gln624His
NM_001621.4:c.1872A>C NP_001612.1:p.Gln624His
NM_001621.5:c.1872A>C MANE Select NP_001612.1:p.Gln624His