Canonical Allele Identifier: CA366895351
Gene: AHR HGNC NCBI

Linked Data

MyVariant Identifiers: chr7:g.17379308A>G (hg19) chr7:g.17339684A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.17339684A>G , CM000669.2:g.17339684A>G GRCh38
NC_000007.13:g.17379308A>G , CM000669.1:g.17379308A>G GRCh37
NC_000007.12:g.17345833A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000242057.9:c.1859A>G MANE Select ENSP00000242057.4:p.Glu620Gly
ENST00000637807.1:c.1829A>G ENSP00000490530.1:p.Glu610Gly
ENST00000642825.1:c.1814A>G ENSP00000495987.1:p.Glu605Gly
ENST00000242057.8:c.1859A>G ENSP00000242057.4:p.Glu620Gly
ENST00000463496.1:c.1859A>G ENSP00000436466.1:p.Glu620Gly
NM_001621.4:c.1859A>G NP_001612.1:p.Glu620Gly
NM_001621.5:c.1859A>G MANE Select NP_001612.1:p.Glu620Gly
Search 100 bp 5'
Search 100 bp 3'