Canonical Allele Identifier: CA1691323921

Gene: AHR

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.17339667G= , CM000669.2:g.17339667G=	GRCh38
NC_000007.13:g.17379291G= , CM000669.1:g.17379291G=	GRCh37
NC_000007.12:g.17345816G=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000242057.9:c.1842G= MANE Select	ENSP00000242057.4:p.Gln614=
ENST00000637807.1:c.1812G=	ENSP00000490530.1:p.Gln604=
ENST00000642825.1:c.1797G=	ENSP00000495987.1:p.Gln599=
ENST00000242057.8:c.1842G=	ENSP00000242057.4:p.Gln614=
ENST00000463496.1:c.1842G=	ENSP00000436466.1:p.Gln614=
NM_001621.4:c.1842G=	NP_001612.1:p.Gln614=
NM_001621.5:c.1842G= MANE Select	NP_001612.1:p.Gln614=