Canonical Allele Identifier: CA375576098

Gene: AGPAT2

Linked Data

• dbSNP Id: rs1452388592
• gnomAD v3: 9-136673765-T-G
• gnomAD v4: 9-136673765-T-G
• MyVariant Identifiers: chr9:g.139568217T>G (hg19) ; chr9:g.136673765T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.136673765T>G , CM000671.2:g.136673765T>G	GRCh38
NC_000009.11:g.139568217T>G , CM000671.1:g.139568217T>G	GRCh37
NC_000009.10:g.138688038T>G	NCBI36
NG_008090.1:g.18695A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371696.7:c.824A>C MANE Select	ENSP00000360761.2:p.Gln275Pro
ENST00000371694.7:c.728A>C	ENSP00000360759.3:p.Gln243Pro
ENST00000371696.6:c.824A>C	ENSP00000360761.2:p.Gln275Pro
ENST00000472820.1:n.752A>C
ENST00000538402.1:c.824A>C	ENSP00000438919.1:p.Gln275Pro
NM_001012727.1:c.728A>C	NP_001012745.1:p.Gln243Pro
NM_006412.3:c.824A>C	NP_006403.2:p.Gln275Pro
NM_006412.4:c.824A>C MANE Select	NP_006403.2:p.Gln275Pro
NM_001012727.2:c.728A>C	NP_001012745.1:p.Gln243Pro