Canonical Allele Identifier: CA154100890

Gene: AHR

Linked Data - Predicted Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.17318249T>A , CM000669.2:g.17318249T>A	GRCh38
NC_000007.13:g.17357873T>A , CM000669.1:g.17357873T>A	GRCh37
NC_000007.12:g.17324398T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000242057.9:c.254-4252T>A MANE Select	ENSP00000242057.4:n.254-4252T>A
ENST00000637807.1:c.224-4252T>A	ENSP00000490530.1:n.224-4252T>A
ENST00000642825.1:c.209-4252T>A	ENSP00000495987.1:n.209-4252T>A
ENST00000242057.8:c.254-4252T>A	ENSP00000242057.4:n.254-4252T>A
ENST00000463496.1:c.254-4252T>A	ENSP00000436466.1:n.254-4252T>A
NM_001621.4:c.254-4252T>A	NP_001612.1:n.254-4252T>A
NM_001621.5:c.254-4252T>A MANE Select	NP_001612.1:n.254-4252T>A