Canonical Allele Identifier: CA366895560
Gene: AHR HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.17339770G>C , CM000669.2:g.17339770G>C GRCh38
NC_000007.13:g.17379394G>C , CM000669.1:g.17379394G>C GRCh37
NC_000007.12:g.17345919G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000242057.9:c.1945G>C MANE Select ENSP00000242057.4:p.Gly649Arg
ENST00000637807.1:c.1915G>C ENSP00000490530.1:p.Gly639Arg
ENST00000642825.1:c.1900G>C ENSP00000495987.1:p.Gly634Arg
ENST00000242057.8:c.1945G>C ENSP00000242057.4:p.Gly649Arg
ENST00000463496.1:c.1945G>C ENSP00000436466.1:p.Gly649Arg
NM_001621.4:c.1945G>C NP_001612.1:p.Gly649Arg
NM_001621.5:c.1945G>C MANE Select NP_001612.1:p.Gly649Arg