Canonical Allele Identifier: CA366895530

Gene: AHR

Linked Data

• gnomAD v4: 7-17339758-A-T
• MyVariant Identifiers: chr7:g.17379382A>T (hg19) ; chr7:g.17339758A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.17339758A>T , CM000669.2:g.17339758A>T	GRCh38
NC_000007.13:g.17379382A>T , CM000669.1:g.17379382A>T	GRCh37
NC_000007.12:g.17345907A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000242057.9:c.1933A>T MANE Select	ENSP00000242057.4:p.Met645Leu
ENST00000637807.1:c.1903A>T	ENSP00000490530.1:p.Met635Leu
ENST00000642825.1:c.1888A>T	ENSP00000495987.1:p.Met630Leu
ENST00000242057.8:c.1933A>T	ENSP00000242057.4:p.Met645Leu
ENST00000463496.1:c.1933A>T	ENSP00000436466.1:p.Met645Leu
NM_001621.4:c.1933A>T	NP_001612.1:p.Met645Leu
NM_001621.5:c.1933A>T MANE Select	NP_001612.1:p.Met645Leu