Canonical Allele Identifier: CA366895166

Gene: AHR

Linked Data

• gnomAD v4: 7-17339600-C-T
• MyVariant Identifiers: chr7:g.17379224C>T (hg19) ; chr7:g.17339600C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.17339600C>T , CM000669.2:g.17339600C>T	GRCh38
NC_000007.13:g.17379224C>T , CM000669.1:g.17379224C>T	GRCh37
NC_000007.12:g.17345749C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000242057.9:c.1775C>T MANE Select	ENSP00000242057.4:p.Ser592Phe
ENST00000637807.1:c.1745C>T	ENSP00000490530.1:p.Ser582Phe
ENST00000642825.1:c.1730C>T	ENSP00000495987.1:p.Ser577Phe
ENST00000242057.8:c.1775C>T	ENSP00000242057.4:p.Ser592Phe
ENST00000463496.1:c.1775C>T	ENSP00000436466.1:p.Ser592Phe
NM_001621.4:c.1775C>T	NP_001612.1:p.Ser592Phe
NM_001621.5:c.1775C>T MANE Select	NP_001612.1:p.Ser592Phe