Canonical Allele Identifier: CA467744246

Gene: AGPAT2

Linked Data

• MyVariant Identifiers: chr9:g.139581756C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.136687304C>G , CM000671.2:g.136687304C>G	GRCh38
NC_000009.11:g.139581756C>G , CM000671.1:g.139581756C>G	GRCh37
NC_000009.10:g.138701577C>G	NCBI36
NG_008090.1:g.5156G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371696.7:c.54G>C MANE Select	ENSP00000360761.2:p.Val18=
ENST00000371694.7:c.54G>C	ENSP00000360759.3:p.Val18=
ENST00000371696.6:c.54G>C	ENSP00000360761.2:p.Val18=
ENST00000470861.1:n.62G>C
ENST00000538402.1:c.54G>C	ENSP00000438919.1:p.Val18=
NM_001012727.1:c.54G>C	NP_001012745.1:p.Val18=
NM_006412.3:c.54G>C	NP_006403.2:p.Val18=
NM_006412.4:c.54G>C MANE Select	NP_006403.2:p.Val18=
NM_001012727.2:c.54G>C	NP_001012745.1:p.Val18=