Canonical Allele Identifier: CA366895703

Gene: AHR

Linked Data

• gnomAD v4: 7-17339830-C-T
• MyVariant Identifiers: chr7:g.17379454C>T (hg19) ; chr7:g.17339830C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.17339830C>T , CM000669.2:g.17339830C>T	GRCh38
NC_000007.13:g.17379454C>T , CM000669.1:g.17379454C>T	GRCh37
NC_000007.12:g.17345979C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000242057.9:c.2005C>T MANE Select	ENSP00000242057.4:p.Pro669Ser
ENST00000637807.1:c.1975C>T	ENSP00000490530.1:p.Pro659Ser
ENST00000642825.1:c.1960C>T	ENSP00000495987.1:p.Pro654Ser
ENST00000242057.8:c.2005C>T	ENSP00000242057.4:p.Pro669Ser
ENST00000463496.1:c.2005C>T	ENSP00000436466.1:p.Pro669Ser
NM_001621.4:c.2005C>T	NP_001612.1:p.Pro669Ser
NM_001621.5:c.2005C>T MANE Select	NP_001612.1:p.Pro669Ser