Canonical Allele Identifier: CA375577306

Gene: AGPAT2

Linked Data

• dbSNP Id: rs767338891
• MyVariant Identifiers: chr9:g.139568293G>C (hg19) ; chr9:g.136673841G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.136673841G>C , CM000671.2:g.136673841G>C	GRCh38
NC_000009.11:g.139568293G>C , CM000671.1:g.139568293G>C	GRCh37
NC_000009.10:g.138688114G>C	NCBI36
NG_008090.1:g.18619C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371696.7:c.748C>G MANE Select	ENSP00000360761.2:p.Arg250Gly
ENST00000371694.7:c.652C>G	ENSP00000360759.3:p.Arg218Gly
ENST00000371696.6:c.748C>G	ENSP00000360761.2:p.Arg250Gly
ENST00000472820.1:n.676C>G
ENST00000538402.1:c.748C>G	ENSP00000438919.1:p.Arg250Gly
NM_001012727.1:c.652C>G	NP_001012745.1:p.Arg218Gly
NM_006412.3:c.748C>G	NP_006403.2:p.Arg250Gly
NM_006412.4:c.748C>G MANE Select	NP_006403.2:p.Arg250Gly
NM_001012727.2:c.652C>G	NP_001012745.1:p.Arg218Gly