Canonical Allele Identifier: CA454134079

Gene: AHR

Linked Data

• gnomAD v4: 7-17339406-C-T
• MyVariant Identifiers: chr7:g.17379030C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.17339406C>T , CM000669.2:g.17339406C>T	GRCh38
NC_000007.13:g.17379030C>T , CM000669.1:g.17379030C>T	GRCh37
NC_000007.12:g.17345555C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000242057.9:c.1581C>T MANE Select	ENSP00000242057.4:p.His527=
ENST00000637807.1:c.1551C>T	ENSP00000490530.1:p.His517=
ENST00000642825.1:c.1536C>T	ENSP00000495987.1:p.His512=
ENST00000242057.8:c.1581C>T	ENSP00000242057.4:p.His527=
ENST00000463496.1:c.1581C>T	ENSP00000436466.1:p.His527=
ENST00000492120.1:n.563C>T
NM_001621.4:c.1581C>T	NP_001612.1:p.His527=
NM_001621.5:c.1581C>T MANE Select	NP_001612.1:p.His527=