Canonical Allele Identifier: CA366894702

Gene: AHR

Linked Data

• dbSNP Id: rs1426667272
• gnomAD v2: 7-17379073-A-G
• gnomAD v4: 7-17339449-A-G
• MyVariant Identifiers: chr7:g.17379073A>G (hg19) ; chr7:g.17339449A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.17339449A>G , CM000669.2:g.17339449A>G	GRCh38
NC_000007.13:g.17379073A>G , CM000669.1:g.17379073A>G	GRCh37
NC_000007.12:g.17345598A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000242057.9:c.1624A>G MANE Select	ENSP00000242057.4:p.Ile542Val
ENST00000637807.1:c.1594A>G	ENSP00000490530.1:p.Ile532Val
ENST00000642825.1:c.1579A>G	ENSP00000495987.1:p.Ile527Val
ENST00000242057.8:c.1624A>G	ENSP00000242057.4:p.Ile542Val
ENST00000463496.1:c.1624A>G	ENSP00000436466.1:p.Ile542Val
ENST00000492120.1:n.606A>G
NM_001621.4:c.1624A>G	NP_001612.1:p.Ile542Val
NM_001621.5:c.1624A>G MANE Select	NP_001612.1:p.Ile542Val