Canonical Allele Identifier: CA366895756
Gene: AHR HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.17339852C>T , CM000669.2:g.17339852C>T GRCh38
NC_000007.13:g.17379476C>T , CM000669.1:g.17379476C>T GRCh37
NC_000007.12:g.17346001C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000242057.9:c.2027C>T MANE Select ENSP00000242057.4:p.Thr676Ile
ENST00000637807.1:c.1997C>T ENSP00000490530.1:p.Thr666Ile
ENST00000642825.1:c.1982C>T ENSP00000495987.1:p.Thr661Ile
ENST00000242057.8:c.2027C>T ENSP00000242057.4:p.Thr676Ile
ENST00000463496.1:c.2027C>T ENSP00000436466.1:p.Thr676Ile
NM_001621.4:c.2027C>T NP_001612.1:p.Thr676Ile
NM_001621.5:c.2027C>T MANE Select NP_001612.1:p.Thr676Ile