Canonical Allele Identifier: CA366895606

Gene: AHR

Linked Data

• gnomAD v4: 7-17339789-A-G
• MyVariant Identifiers: chr7:g.17379413A>G (hg19) ; chr7:g.17339789A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.17339789A>G , CM000669.2:g.17339789A>G	GRCh38
NC_000007.13:g.17379413A>G , CM000669.1:g.17379413A>G	GRCh37
NC_000007.12:g.17345938A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000242057.9:c.1964A>G MANE Select	ENSP00000242057.4:p.Asn655Ser
ENST00000637807.1:c.1934A>G	ENSP00000490530.1:p.Asn645Ser
ENST00000642825.1:c.1919A>G	ENSP00000495987.1:p.Asn640Ser
ENST00000242057.8:c.1964A>G	ENSP00000242057.4:p.Asn655Ser
ENST00000463496.1:c.1964A>G	ENSP00000436466.1:p.Asn655Ser
NM_001621.4:c.1964A>G	NP_001612.1:p.Asn655Ser
NM_001621.5:c.1964A>G MANE Select	NP_001612.1:p.Asn655Ser