Canonical Allele Identifier: CA366895658
Gene: AHR HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.17339812A>C , CM000669.2:g.17339812A>C GRCh38
NC_000007.13:g.17379436A>C , CM000669.1:g.17379436A>C GRCh37
NC_000007.12:g.17345961A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000242057.9:c.1987A>C MANE Select ENSP00000242057.4:p.Asn663His
ENST00000637807.1:c.1957A>C ENSP00000490530.1:p.Asn653His
ENST00000642825.1:c.1942A>C ENSP00000495987.1:p.Asn648His
ENST00000242057.8:c.1987A>C ENSP00000242057.4:p.Asn663His
ENST00000463496.1:c.1987A>C ENSP00000436466.1:p.Asn663His
NM_001621.4:c.1987A>C NP_001612.1:p.Asn663His
NM_001621.5:c.1987A>C MANE Select NP_001612.1:p.Asn663His