Canonical Allele Identifier: CA375587868
Gene: AGPAT2 HGNC NCBI

Linked Data

dbSNP Id: rs1239418038

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.136687188A>T , CM000671.2:g.136687188A>T GRCh38
NC_000009.11:g.139581640A>T , CM000671.1:g.139581640A>T GRCh37
NC_000009.10:g.138701461A>T NCBI36
NG_008090.1:g.5272T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000371696.7:c.170T>A MANE Select ENSP00000360761.2:p.Val57Glu
ENST00000371694.7:c.170T>A ENSP00000360759.3:p.Val57Glu
ENST00000371696.6:c.170T>A ENSP00000360761.2:p.Val57Glu
ENST00000470861.1:n.178T>A
ENST00000538402.1:c.170T>A ENSP00000438919.1:p.Val57Glu
NM_001012727.1:c.170T>A NP_001012745.1:p.Val57Glu
NM_006412.3:c.170T>A NP_006403.2:p.Val57Glu
NM_006412.4:c.170T>A MANE Select NP_006403.2:p.Val57Glu
NM_001012727.2:c.170T>A NP_001012745.1:p.Val57Glu