Canonical Allele Identifier: CA1691323854

Gene: AHR

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.17339491A= , CM000669.2:g.17339491A=	GRCh38
NC_000007.13:g.17379115A= , CM000669.1:g.17379115A=	GRCh37
NC_000007.12:g.17345640A=	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000242057.9:c.1666A= MANE Select	ENSP00000242057.4:p.Met556=
ENST00000637807.1:c.1636A=	ENSP00000490530.1:p.Met546=
ENST00000642825.1:c.1621A=	ENSP00000495987.1:p.Met541=
ENST00000242057.8:c.1666A=	ENSP00000242057.4:p.Met556=
ENST00000463496.1:c.1666A=	ENSP00000436466.1:p.Met556=
ENST00000492120.1:n.648A=
NM_001621.4:c.1666A=	NP_001612.1:p.Met556=
NM_001621.5:c.1666A= MANE Select	NP_001612.1:p.Met556=