Canonical Allele Identifier: CA375588177

Gene: AGPAT2

Linked Data

• dbSNP Id: rs1360933401
• gnomAD v2: 9-139581722-C-T
• gnomAD v4: 9-136687270-C-T
• MyVariant Identifiers: chr9:g.139581722C>T (hg19) ; chr9:g.136687270C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.136687270C>T , CM000671.2:g.136687270C>T	GRCh38
NC_000009.11:g.139581722C>T , CM000671.1:g.139581722C>T	GRCh37
NC_000009.10:g.138701543C>T	NCBI36
NG_008090.1:g.5190G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371696.7:c.88G>A MANE Select	ENSP00000360761.2:p.Val30Ile
ENST00000371694.7:c.88G>A	ENSP00000360759.3:p.Val30Ile
ENST00000371696.6:c.88G>A	ENSP00000360761.2:p.Val30Ile
ENST00000470861.1:n.96G>A
ENST00000538402.1:c.88G>A	ENSP00000438919.1:p.Val30Ile
NM_001012727.1:c.88G>A	NP_001012745.1:p.Val30Ile
NM_006412.3:c.88G>A	NP_006403.2:p.Val30Ile
NM_006412.4:c.88G>A MANE Select	NP_006403.2:p.Val30Ile
NM_001012727.2:c.88G>A	NP_001012745.1:p.Val30Ile