Canonical Allele Identifier: CA366895638

Gene: AHR

Linked Data

• gnomAD v4: 7-17339802-C-G
• MyVariant Identifiers: chr7:g.17379426C>G (hg19) ; chr7:g.17339802C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.17339802C>G , CM000669.2:g.17339802C>G	GRCh38
NC_000007.13:g.17379426C>G , CM000669.1:g.17379426C>G	GRCh37
NC_000007.12:g.17345951C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000242057.9:c.1977C>G MANE Select	ENSP00000242057.4:p.Phe659Leu
ENST00000637807.1:c.1947C>G	ENSP00000490530.1:p.Phe649Leu
ENST00000642825.1:c.1932C>G	ENSP00000495987.1:p.Phe644Leu
ENST00000242057.8:c.1977C>G	ENSP00000242057.4:p.Phe659Leu
ENST00000463496.1:c.1977C>G	ENSP00000436466.1:p.Phe659Leu
NM_001621.4:c.1977C>G	NP_001612.1:p.Phe659Leu
NM_001621.5:c.1977C>G MANE Select	NP_001612.1:p.Phe659Leu