Canonical Allele Identifier: CA366895230

Gene: AHR

Linked Data

• gnomAD v4: 7-17339629-C-T
• MyVariant Identifiers: chr7:g.17379253C>T (hg19) ; chr7:g.17339629C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.17339629C>T , CM000669.2:g.17339629C>T	GRCh38
NC_000007.13:g.17379253C>T , CM000669.1:g.17379253C>T	GRCh37
NC_000007.12:g.17345778C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000242057.9:c.1804C>T MANE Select	ENSP00000242057.4:p.Gln602Ter
ENST00000637807.1:c.1774C>T	ENSP00000490530.1:p.Gln592Ter
ENST00000642825.1:c.1759C>T	ENSP00000495987.1:p.Gln587Ter
ENST00000242057.8:c.1804C>T	ENSP00000242057.4:p.Gln602Ter
ENST00000463496.1:c.1804C>T	ENSP00000436466.1:p.Gln602Ter
NM_001621.4:c.1804C>T	NP_001612.1:p.Gln602Ter
NM_001621.5:c.1804C>T MANE Select	NP_001612.1:p.Gln602Ter