Canonical Allele Identifier: CA1691323944
Gene: AHR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.17339720T= , CM000669.2:g.17339720T= GRCh38
NC_000007.13:g.17379344T= , CM000669.1:g.17379344T= GRCh37
NC_000007.12:g.17345869T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000242057.9:c.1895T= MANE Select ENSP00000242057.4:p.Val632=
ENST00000637807.1:c.1865T= ENSP00000490530.1:p.Val622=
ENST00000642825.1:c.1850T= ENSP00000495987.1:p.Val617=
ENST00000242057.8:c.1895T= ENSP00000242057.4:p.Val632=
ENST00000463496.1:c.1895T= ENSP00000436466.1:p.Val632=
NM_001621.4:c.1895T= NP_001612.1:p.Val632=
NM_001621.5:c.1895T= MANE Select NP_001612.1:p.Val632=