Canonical Allele Identifier: CA366895753
Gene: AHR HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.17339851A>G , CM000669.2:g.17339851A>G GRCh38
NC_000007.13:g.17379475A>G , CM000669.1:g.17379475A>G GRCh37
NC_000007.12:g.17346000A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000242057.9:c.2026A>G MANE Select ENSP00000242057.4:p.Thr676Ala
ENST00000637807.1:c.1996A>G ENSP00000490530.1:p.Thr666Ala
ENST00000642825.1:c.1981A>G ENSP00000495987.1:p.Thr661Ala
ENST00000242057.8:c.2026A>G ENSP00000242057.4:p.Thr676Ala
ENST00000463496.1:c.2026A>G ENSP00000436466.1:p.Thr676Ala
NM_001621.4:c.2026A>G NP_001612.1:p.Thr676Ala
NM_001621.5:c.2026A>G MANE Select NP_001612.1:p.Thr676Ala