Canonical Allele Identifier: CA366895758

Gene: AHR

Linked Data

• gnomAD v4: 7-17339854-G-T
• MyVariant Identifiers: chr7:g.17379478G>T (hg19) ; chr7:g.17339854G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.17339854G>T , CM000669.2:g.17339854G>T	GRCh38
NC_000007.13:g.17379478G>T , CM000669.1:g.17379478G>T	GRCh37
NC_000007.12:g.17346003G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000242057.9:c.2029G>T MANE Select	ENSP00000242057.4:p.Asp677Tyr
ENST00000637807.1:c.1999G>T	ENSP00000490530.1:p.Asp667Tyr
ENST00000642825.1:c.1984G>T	ENSP00000495987.1:p.Asp662Tyr
ENST00000242057.8:c.2029G>T	ENSP00000242057.4:p.Asp677Tyr
ENST00000463496.1:c.2029G>T	ENSP00000436466.1:p.Asp677Tyr
NM_001621.4:c.2029G>T	NP_001612.1:p.Asp677Tyr
NM_001621.5:c.2029G>T MANE Select	NP_001612.1:p.Asp677Tyr