Canonical Allele Identifier: CA454134392

Gene: AHR

Linked Data

• MyVariant Identifiers: chr7:g.17379456A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.17339832A>T , CM000669.2:g.17339832A>T	GRCh38
NC_000007.13:g.17379456A>T , CM000669.1:g.17379456A>T	GRCh37
NC_000007.12:g.17345981A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000242057.9:c.2007A>T MANE Select	ENSP00000242057.4:p.Pro669=
ENST00000637807.1:c.1977A>T	ENSP00000490530.1:p.Pro659=
ENST00000642825.1:c.1962A>T	ENSP00000495987.1:p.Pro654=
ENST00000242057.8:c.2007A>T	ENSP00000242057.4:p.Pro669=
ENST00000463496.1:c.2007A>T	ENSP00000436466.1:p.Pro669=
NM_001621.4:c.2007A>T	NP_001612.1:p.Pro669=
NM_001621.5:c.2007A>T MANE Select	NP_001612.1:p.Pro669=