Canonical Allele Identifier: CA366895747
Gene: AHR HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.17339849T>C , CM000669.2:g.17339849T>C GRCh38
NC_000007.13:g.17379473T>C , CM000669.1:g.17379473T>C GRCh37
NC_000007.12:g.17345998T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000242057.9:c.2024T>C MANE Select ENSP00000242057.4:p.Phe675Ser
ENST00000637807.1:c.1994T>C ENSP00000490530.1:p.Phe665Ser
ENST00000642825.1:c.1979T>C ENSP00000495987.1:p.Phe660Ser
ENST00000242057.8:c.2024T>C ENSP00000242057.4:p.Phe675Ser
ENST00000463496.1:c.2024T>C ENSP00000436466.1:p.Phe675Ser
NM_001621.4:c.2024T>C NP_001612.1:p.Phe675Ser
NM_001621.5:c.2024T>C MANE Select NP_001612.1:p.Phe675Ser