Canonical Allele Identifier: CA454134202

Gene: AHR

Linked Data

• MyVariant Identifiers: chr7:g.17379288A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.17339664A>T , CM000669.2:g.17339664A>T	GRCh38
NC_000007.13:g.17379288A>T , CM000669.1:g.17379288A>T	GRCh37
NC_000007.12:g.17345813A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000242057.9:c.1839A>T MANE Select	ENSP00000242057.4:p.Val613=
ENST00000637807.1:c.1809A>T	ENSP00000490530.1:p.Val603=
ENST00000642825.1:c.1794A>T	ENSP00000495987.1:p.Val598=
ENST00000242057.8:c.1839A>T	ENSP00000242057.4:p.Val613=
ENST00000463496.1:c.1839A>T	ENSP00000436466.1:p.Val613=
NM_001621.4:c.1839A>T	NP_001612.1:p.Val613=
NM_001621.5:c.1839A>T MANE Select	NP_001612.1:p.Val613=