Canonical Allele Identifier: CA366895332

Gene: AHR

Linked Data

• dbSNP Id: rs1782397508
• MyVariant Identifiers: chr7:g.17379298C>G (hg19) ; chr7:g.17339674C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.17339674C>G , CM000669.2:g.17339674C>G	GRCh38
NC_000007.13:g.17379298C>G , CM000669.1:g.17379298C>G	GRCh37
NC_000007.12:g.17345823C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000242057.9:c.1849C>G MANE Select	ENSP00000242057.4:p.Leu617Val
ENST00000637807.1:c.1819C>G	ENSP00000490530.1:p.Leu607Val
ENST00000642825.1:c.1804C>G	ENSP00000495987.1:p.Leu602Val
ENST00000242057.8:c.1849C>G	ENSP00000242057.4:p.Leu617Val
ENST00000463496.1:c.1849C>G	ENSP00000436466.1:p.Leu617Val
NM_001621.4:c.1849C>G	NP_001612.1:p.Leu617Val
NM_001621.5:c.1849C>G MANE Select	NP_001612.1:p.Leu617Val