Canonical Allele Identifier: CA366894491
Gene: AHR HGNC NCBI

Linked Data

gnomAD v4: 7-17339407-C-G

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.17339407C>G , CM000669.2:g.17339407C>G GRCh38
NC_000007.13:g.17379031C>G , CM000669.1:g.17379031C>G GRCh37
NC_000007.12:g.17345556C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000242057.9:c.1582C>G MANE Select ENSP00000242057.4:p.Pro528Ala
ENST00000637807.1:c.1552C>G ENSP00000490530.1:p.Pro518Ala
ENST00000642825.1:c.1537C>G ENSP00000495987.1:p.Pro513Ala
ENST00000242057.8:c.1582C>G ENSP00000242057.4:p.Pro528Ala
ENST00000463496.1:c.1582C>G ENSP00000436466.1:p.Pro528Ala
ENST00000492120.1:n.564C>G
NM_001621.4:c.1582C>G NP_001612.1:p.Pro528Ala
NM_001621.5:c.1582C>G MANE Select NP_001612.1:p.Pro528Ala