Canonical Allele Identifier: CA2603866190
Gene: AGPAT2 HGNC NCBI

Linked Data

dbSNP Id: rs1846053322
gnomAD v3: 9-136674057-C-T
gnomAD v4: 9-136674057-C-T
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.136674057C>T , CM000671.2:g.136674057C>T GRCh38
NC_000009.11:g.139568509C>T , CM000671.1:g.139568509C>T GRCh37
NC_000009.10:g.138688330C>T NCBI36
NG_008090.1:g.18403G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000371696.7:c.662-130G>A MANE Select ENSP00000360761.2:n.662-130G>A
ENST00000371694.7:c.566-130G>A ENSP00000360759.3:n.566-130G>A
ENST00000371696.6:c.662-130G>A ENSP00000360761.2:n.662-130G>A
ENST00000472820.1:n.590-130G>A
ENST00000538402.1:c.662-130G>A ENSP00000438919.1:n.662-130G>A
NM_001012727.1:c.566-130G>A NP_001012745.1:n.566-130G>A
NM_006412.3:c.662-130G>A NP_006403.2:n.662-130G>A
NM_006412.4:c.662-130G>A MANE Select NP_006403.2:n.662-130G>A
NM_001012727.2:c.566-130G>A NP_001012745.1:n.566-130G>A
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