Canonical Allele Identifier: CA1691323977
Gene: AHR HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.17339814T= , CM000669.2:g.17339814T= GRCh38
NC_000007.13:g.17379438T= , CM000669.1:g.17379438T= GRCh37
NC_000007.12:g.17345963T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000242057.9:c.1989T= MANE Select ENSP00000242057.4:p.Asn663=
ENST00000637807.1:c.1959T= ENSP00000490530.1:p.Asn653=
ENST00000642825.1:c.1944T= ENSP00000495987.1:p.Asn648=
ENST00000242057.8:c.1989T= ENSP00000242057.4:p.Asn663=
ENST00000463496.1:c.1989T= ENSP00000436466.1:p.Asn663=
NM_001621.4:c.1989T= NP_001612.1:p.Asn663=
NM_001621.5:c.1989T= MANE Select NP_001612.1:p.Asn663=
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