Canonical Allele Identifier: CA467738173
Gene: AGPAT2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr9:g.139569221G>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.136674769G>T , CM000671.2:g.136674769G>T GRCh38
NC_000009.11:g.139569221G>T , CM000671.1:g.139569221G>T GRCh37
NC_000009.10:g.138689042G>T NCBI36
NG_008090.1:g.17691C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000371696.7:c.627C>A MANE Select ENSP00000360761.2:p.Ser209=
ENST00000371694.7:c.531C>A ENSP00000360759.3:p.Ser177=
ENST00000371696.6:c.627C>A ENSP00000360761.2:p.Ser209=
ENST00000472820.1:n.555C>A
ENST00000538402.1:c.627C>A ENSP00000438919.1:p.Ser209=
NM_001012727.1:c.531C>A NP_001012745.1:p.Ser177=
NM_006412.3:c.627C>A NP_006403.2:p.Ser209=
NM_006412.4:c.627C>A MANE Select NP_006403.2:p.Ser209=
NM_001012727.2:c.531C>A NP_001012745.1:p.Ser177=