Canonical Allele Identifier: CA366894770

Gene: AHR

Linked Data

• dbSNP Id: rs1452709012
• gnomAD v2: 7-17379085-C-G
• MyVariant Identifiers: chr7:g.17379085C>G (hg19) ; chr7:g.17339461C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.17339461C>G , CM000669.2:g.17339461C>G	GRCh38
NC_000007.13:g.17379085C>G , CM000669.1:g.17379085C>G	GRCh37
NC_000007.12:g.17345610C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000242057.9:c.1636C>G MANE Select	ENSP00000242057.4:p.Leu546Val
ENST00000637807.1:c.1606C>G	ENSP00000490530.1:p.Leu536Val
ENST00000642825.1:c.1591C>G	ENSP00000495987.1:p.Leu531Val
ENST00000242057.8:c.1636C>G	ENSP00000242057.4:p.Leu546Val
ENST00000463496.1:c.1636C>G	ENSP00000436466.1:p.Leu546Val
ENST00000492120.1:n.618C>G
NM_001621.4:c.1636C>G	NP_001612.1:p.Leu546Val
NM_001621.5:c.1636C>G MANE Select	NP_001612.1:p.Leu546Val