Canonical Allele Identifier: CA4172221
Gene: AHR HGNC NCBI

Linked Data

ClinVar Variation Id: 1015449
ClinVar RCV Id: RCV001314311 RCV004034310
dbSNP Id: rs753313211
ExAC: 7:17379469 G / A
gnomAD v2: 7-17379469-G-A
gnomAD v3: 7-17339845-G-A
gnomAD v4: 7-17339845-G-A
MyVariant Identifiers: chr7:g.17379469G>A (hg19) chr7:g.17339845G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.17339845G>A , CM000669.2:g.17339845G>A GRCh38
NC_000007.13:g.17379469G>A , CM000669.1:g.17379469G>A GRCh37
NC_000007.12:g.17345994G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000242057.9:c.2020G>A MANE Select ENSP00000242057.4:p.Val674Ile
ENST00000637807.1:c.1990G>A ENSP00000490530.1:p.Val664Ile
ENST00000642825.1:c.1975G>A ENSP00000495987.1:p.Val659Ile
ENST00000242057.8:c.2020G>A ENSP00000242057.4:p.Val674Ile
ENST00000463496.1:c.2020G>A ENSP00000436466.1:p.Val674Ile
NM_001621.4:c.2020G>A NP_001612.1:p.Val674Ile
NM_001621.5:c.2020G>A MANE Select NP_001612.1:p.Val674Ile
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