Canonical Allele Identifier: CA366895489
Gene: AHR HGNC NCBI

Linked Data

ClinVar Variation Id: 1713835
ClinVar RCV Id: RCV002303120
MyVariant Identifiers: chr7:g.17379367C>G (hg19) chr7:g.17339743C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.17339743C>G , CM000669.2:g.17339743C>G GRCh38
NC_000007.13:g.17379367C>G , CM000669.1:g.17379367C>G GRCh37
NC_000007.12:g.17345892C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000242057.9:c.1918C>G MANE Select ENSP00000242057.4:p.Gln640Glu
ENST00000637807.1:c.1888C>G ENSP00000490530.1:p.Gln630Glu
ENST00000642825.1:c.1873C>G ENSP00000495987.1:p.Gln625Glu
ENST00000242057.8:c.1918C>G ENSP00000242057.4:p.Gln640Glu
ENST00000463496.1:c.1918C>G ENSP00000436466.1:p.Gln640Glu
NM_001621.4:c.1918C>G NP_001612.1:p.Gln640Glu
NM_001621.5:c.1918C>G MANE Select NP_001612.1:p.Gln640Glu
Search 100 bp 5'
Search 100 bp 3'