Canonical Allele Identifier: CA454134233
Gene: AHR HGNC NCBI

Linked Data

dbSNP Id: rs1782398197
gnomAD v4: 7-17339724-G-A
MyVariant Identifiers: chr7:g.17379348G>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.17339724G>A , CM000669.2:g.17339724G>A GRCh38
NC_000007.13:g.17379348G>A , CM000669.1:g.17379348G>A GRCh37
NC_000007.12:g.17345873G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000242057.9:c.1899G>A MANE Select ENSP00000242057.4:p.Glu633=
ENST00000637807.1:c.1869G>A ENSP00000490530.1:p.Glu623=
ENST00000642825.1:c.1854G>A ENSP00000495987.1:p.Glu618=
ENST00000242057.8:c.1899G>A ENSP00000242057.4:p.Glu633=
ENST00000463496.1:c.1899G>A ENSP00000436466.1:p.Glu633=
NM_001621.4:c.1899G>A NP_001612.1:p.Glu633=
NM_001621.5:c.1899G>A MANE Select NP_001612.1:p.Glu633=
Search 100 bp 5'
Search 100 bp 3'