Canonical Allele Identifier: CA1691323821

Gene: AHR

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.17339423A= , CM000669.2:g.17339423A=	GRCh38
NC_000007.13:g.17379047A= , CM000669.1:g.17379047A=	GRCh37
NC_000007.12:g.17345572A=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000242057.9:c.1598A= MANE Select	ENSP00000242057.4:p.Asp533=
ENST00000637807.1:c.1568A=	ENSP00000490530.1:p.Asp523=
ENST00000642825.1:c.1553A=	ENSP00000495987.1:p.Asp518=
ENST00000242057.8:c.1598A=	ENSP00000242057.4:p.Asp533=
ENST00000463496.1:c.1598A=	ENSP00000436466.1:p.Asp533=
ENST00000492120.1:n.580A=
NM_001621.4:c.1598A=	NP_001612.1:p.Asp533=
NM_001621.5:c.1598A= MANE Select	NP_001612.1:p.Asp533=