Canonical Allele Identifier: CA1691323919
Gene: AHR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.17339655C= , CM000669.2:g.17339655C= GRCh38
NC_000007.13:g.17379279C= , CM000669.1:g.17379279C= GRCh37
NC_000007.12:g.17345804C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000242057.9:c.1830C= MANE Select ENSP00000242057.4:p.Ser610=
ENST00000637807.1:c.1800C= ENSP00000490530.1:p.Ser600=
ENST00000642825.1:c.1785C= ENSP00000495987.1:p.Ser595=
ENST00000242057.8:c.1830C= ENSP00000242057.4:p.Ser610=
ENST00000463496.1:c.1830C= ENSP00000436466.1:p.Ser610=
NM_001621.4:c.1830C= NP_001612.1:p.Ser610=
NM_001621.5:c.1830C= MANE Select NP_001612.1:p.Ser610=