Canonical Allele Identifier: CA591184508
Gene: AGPAT2 HGNC NCBI

Linked Data

ClinVar Variation Id: 913448
ClinVar RCV Id: RCV001167075
dbSNP Id: rs1187808090
gnomAD v2: 9-139571139-G-A
gnomAD v3: 9-136676687-G-A
gnomAD v4: 9-136676687-G-A
MyVariant Identifiers: chr9:g.139571139G>A (hg19) chr9:g.136676687G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.136676687G>A , CM000671.2:g.136676687G>A GRCh38
NC_000009.11:g.139571139G>A , CM000671.1:g.139571139G>A GRCh37
NC_000009.10:g.138690960G>A NCBI36
NG_008090.1:g.15773C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000371696.7:c.493-7C>T MANE Select ENSP00000360761.2:n.493-7C>T
ENST00000371694.7:c.492+274C>T ENSP00000360759.3:n.492+274C>T
ENST00000371696.6:c.493-7C>T ENSP00000360761.2:n.493-7C>T
ENST00000472820.1:n.421-7C>T
ENST00000538402.1:c.493-7C>T ENSP00000438919.1:n.493-7C>T
NM_001012727.1:c.492+274C>T NP_001012745.1:n.492+274C>T
NM_006412.3:c.493-7C>T NP_006403.2:n.493-7C>T
NM_006412.4:c.493-7C>T MANE Select NP_006403.2:n.493-7C>T
NM_001012727.2:c.492+274C>T NP_001012745.1:n.492+274C>T
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