Canonical Allele Identifier: CA2681909916
Gene: AHR HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.17339729dup , CM000669.2:g.17339729dup GRCh38
NC_000007.13:g.17379353dup , CM000669.1:g.17379353dup GRCh37
NC_000007.12:g.17345878dup NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000242057.9:c.1904dup MANE Select ENSP00000242057.4:p.Gln636AlafsTer13
ENST00000637807.1:c.1874dup ENSP00000490530.1:p.Gln626AlafsTer13
ENST00000642825.1:c.1859dup ENSP00000495987.1:p.Gln621AlafsTer13
ENST00000242057.8:c.1904dup ENSP00000242057.4:p.Gln636AlafsTer13
ENST00000463496.1:c.1904dup ENSP00000436466.1:p.Gln636AlafsTer13
NM_001621.4:c.1904dup NP_001612.1:p.Gln636AlafsTer13
NM_001621.5:c.1904dup MANE Select NP_001612.1:p.Gln636AlafsTer13