Canonical Allele Identifier: CA467738768
Gene: AGPAT2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr9:g.139571082C>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.136676630C>T , CM000671.2:g.136676630C>T GRCh38
NC_000009.11:g.139571082C>T , CM000671.1:g.139571082C>T GRCh37
NC_000009.10:g.138690903C>T NCBI36
NG_008090.1:g.15830G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000371696.7:c.543G>A MANE Select ENSP00000360761.2:p.Leu181=
ENST00000371694.7:c.492+331G>A ENSP00000360759.3:n.492+331G>A
ENST00000371696.6:c.543G>A ENSP00000360761.2:p.Leu181=
ENST00000472820.1:n.471G>A
ENST00000538402.1:c.543G>A ENSP00000438919.1:p.Leu181=
NM_001012727.1:c.492+331G>A NP_001012745.1:n.492+331G>A
NM_006412.3:c.543G>A NP_006403.2:p.Leu181=
NM_006412.4:c.543G>A MANE Select NP_006403.2:p.Leu181=
NM_001012727.2:c.492+331G>A NP_001012745.1:n.492+331G>A
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