Canonical Allele Identifier: CA366895179

Gene: AHR

Linked Data

• MyVariant Identifiers: chr7:g.17379231C>G (hg19) ; chr7:g.17339607C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.17339607C>G , CM000669.2:g.17339607C>G	GRCh38
NC_000007.13:g.17379231C>G , CM000669.1:g.17379231C>G	GRCh37
NC_000007.12:g.17345756C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000242057.9:c.1782C>G MANE Select	ENSP00000242057.4:p.Phe594Leu
ENST00000637807.1:c.1752C>G	ENSP00000490530.1:p.Phe584Leu
ENST00000642825.1:c.1737C>G	ENSP00000495987.1:p.Phe579Leu
ENST00000242057.8:c.1782C>G	ENSP00000242057.4:p.Phe594Leu
ENST00000463496.1:c.1782C>G	ENSP00000436466.1:p.Phe594Leu
NM_001621.4:c.1782C>G	NP_001612.1:p.Phe594Leu
NM_001621.5:c.1782C>G MANE Select	NP_001612.1:p.Phe594Leu