Canonical Allele Identifier: CA4172195
Gene: AHR HGNC NCBI

Linked Data

dbSNP Id: rs763371981
ExAC: 7:17379318 G / A
gnomAD v2: 7-17379318-G-A
gnomAD v3: 7-17339694-G-A
gnomAD v4: 7-17339694-G-A
MyVariant Identifiers: chr7:g.17379318G>A (hg19) chr7:g.17339694G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.17339694G>A , CM000669.2:g.17339694G>A GRCh38
NC_000007.13:g.17379318G>A , CM000669.1:g.17379318G>A GRCh37
NC_000007.12:g.17345843G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000242057.9:c.1869G>A MANE Select ENSP00000242057.4:p.Gln623=
ENST00000637807.1:c.1839G>A ENSP00000490530.1:p.Gln613=
ENST00000642825.1:c.1824G>A ENSP00000495987.1:p.Gln608=
ENST00000242057.8:c.1869G>A ENSP00000242057.4:p.Gln623=
ENST00000463496.1:c.1869G>A ENSP00000436466.1:p.Gln623=
NM_001621.4:c.1869G>A NP_001612.1:p.Gln623=
NM_001621.5:c.1869G>A MANE Select NP_001612.1:p.Gln623=
Search 100 bp 5'
Search 100 bp 3'