Canonical Allele Identifier: CA1691323983
Gene: AHR HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.17339838A= , CM000669.2:g.17339838A= GRCh38
NC_000007.13:g.17379462A= , CM000669.1:g.17379462A= GRCh37
NC_000007.12:g.17345987A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000242057.9:c.2013A= MANE Select ENSP00000242057.4:p.Gln671=
ENST00000637807.1:c.1983A= ENSP00000490530.1:p.Gln661=
ENST00000642825.1:c.1968A= ENSP00000495987.1:p.Gln656=
ENST00000242057.8:c.2013A= ENSP00000242057.4:p.Gln671=
ENST00000463496.1:c.2013A= ENSP00000436466.1:p.Gln671=
NM_001621.4:c.2013A= NP_001612.1:p.Gln671=
NM_001621.5:c.2013A= MANE Select NP_001612.1:p.Gln671=
Search 100 bp 5'
Search 100 bp 3'