Canonical Allele Identifier: CA467738328
Gene: AGPAT2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr9:g.139569248G>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.136674796G>T , CM000671.2:g.136674796G>T GRCh38
NC_000009.11:g.139569248G>T , CM000671.1:g.139569248G>T GRCh37
NC_000009.10:g.138689069G>T NCBI36
NG_008090.1:g.17664C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000371696.7:c.600C>A MANE Select ENSP00000360761.2:p.Val200=
ENST00000371694.7:c.504C>A ENSP00000360759.3:p.Val168=
ENST00000371696.6:c.600C>A ENSP00000360761.2:p.Val200=
ENST00000472820.1:n.528C>A
ENST00000538402.1:c.600C>A ENSP00000438919.1:p.Val200=
NM_001012727.1:c.504C>A NP_001012745.1:p.Val168=
NM_006412.3:c.600C>A NP_006403.2:p.Val200=
NM_006412.4:c.600C>A MANE Select NP_006403.2:p.Val200=
NM_001012727.2:c.504C>A NP_001012745.1:p.Val168=