Canonical Allele Identifier: CA366894781

Gene: AHR

Linked Data

• gnomAD v3: 7-17339464-G-A
• gnomAD v4: 7-17339464-G-A
• MyVariant Identifiers: chr7:g.17379088G>A (hg19) ; chr7:g.17339464G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.17339464G>A , CM000669.2:g.17339464G>A	GRCh38
NC_000007.13:g.17379088G>A , CM000669.1:g.17379088G>A	GRCh37
NC_000007.12:g.17345613G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000242057.9:c.1639G>A MANE Select	ENSP00000242057.4:p.Gly547Ser
ENST00000637807.1:c.1609G>A	ENSP00000490530.1:p.Gly537Ser
ENST00000642825.1:c.1594G>A	ENSP00000495987.1:p.Gly532Ser
ENST00000242057.8:c.1639G>A	ENSP00000242057.4:p.Gly547Ser
ENST00000463496.1:c.1639G>A	ENSP00000436466.1:p.Gly547Ser
ENST00000492120.1:n.621G>A
NM_001621.4:c.1639G>A	NP_001612.1:p.Gly547Ser
NM_001621.5:c.1639G>A MANE Select	NP_001612.1:p.Gly547Ser