Canonical Allele Identifier: CA366894792

Gene: AHR

Linked Data

• dbSNP Id: rs1286907205
• gnomAD v2: 7-17379091-A-G
• gnomAD v4: 7-17339467-A-G
• MyVariant Identifiers: chr7:g.17379091A>G (hg19) ; chr7:g.17339467A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.17339467A>G , CM000669.2:g.17339467A>G	GRCh38
NC_000007.13:g.17379091A>G , CM000669.1:g.17379091A>G	GRCh37
NC_000007.12:g.17345616A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000242057.9:c.1642A>G MANE Select	ENSP00000242057.4:p.Ile548Val
ENST00000637807.1:c.1612A>G	ENSP00000490530.1:p.Ile538Val
ENST00000642825.1:c.1597A>G	ENSP00000495987.1:p.Ile533Val
ENST00000242057.8:c.1642A>G	ENSP00000242057.4:p.Ile548Val
ENST00000463496.1:c.1642A>G	ENSP00000436466.1:p.Ile548Val
ENST00000492120.1:n.624A>G
NM_001621.4:c.1642A>G	NP_001612.1:p.Ile548Val
NM_001621.5:c.1642A>G MANE Select	NP_001612.1:p.Ile548Val