Canonical Allele Identifier: CA591367864

Gene: AGPAT2

Linked Data

• dbSNP Id: rs1305002737
• gnomAD v2: 9-139581581-A-G
• gnomAD v3: 9-136687129-A-G
• gnomAD v4: 9-136687129-A-G
• MyVariant Identifiers: chr9:g.139581581A>G (hg19) ; chr9:g.136687129A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.136687129A>G , CM000671.2:g.136687129A>G	GRCh38
NC_000009.11:g.139581581A>G , CM000671.1:g.139581581A>G	GRCh37
NC_000009.10:g.138701402A>G	NCBI36
NG_008090.1:g.5331T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371696.7:c.182+47T>C MANE Select	ENSP00000360761.2:n.182+47T>C
ENST00000371694.7:c.182+47T>C	ENSP00000360759.3:n.182+47T>C
ENST00000371696.6:c.182+47T>C	ENSP00000360761.2:n.182+47T>C
ENST00000470861.1:n.190+47T>C
ENST00000538402.1:c.182+47T>C	ENSP00000438919.1:n.182+47T>C
NM_001012727.1:c.182+47T>C	NP_001012745.1:n.182+47T>C
NM_006412.3:c.182+47T>C	NP_006403.2:n.182+47T>C
NM_006412.4:c.182+47T>C MANE Select	NP_006403.2:n.182+47T>C
NM_001012727.2:c.182+47T>C	NP_001012745.1:n.182+47T>C