Canonical Allele Identifier: CA5342805

Gene: AGPAT2

Linked Data

• dbSNP Id: rs753350881
• ExAC: 9:139568223 C / G
• gnomAD v2: 9-139568223-C-G
• gnomAD v4: 9-136673771-C-G
• MyVariant Identifiers: chr9:g.139568223C>G (hg19) ; chr9:g.136673771C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.136673771C>G , CM000671.2:g.136673771C>G	GRCh38
NC_000009.11:g.139568223C>G , CM000671.1:g.139568223C>G	GRCh37
NC_000009.10:g.138688044C>G	NCBI36
NG_008090.1:g.18689G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371696.7:c.818G>C MANE Select	ENSP00000360761.2:p.Gly273Ala
ENST00000371694.7:c.722G>C	ENSP00000360759.3:p.Gly241Ala
ENST00000371696.6:c.818G>C	ENSP00000360761.2:p.Gly273Ala
ENST00000472820.1:n.746G>C
ENST00000538402.1:c.818G>C	ENSP00000438919.1:p.Gly273Ala
NM_001012727.1:c.722G>C	NP_001012745.1:p.Gly241Ala
NM_006412.3:c.818G>C	NP_006403.2:p.Gly273Ala
NM_006412.4:c.818G>C MANE Select	NP_006403.2:p.Gly273Ala
NM_001012727.2:c.722G>C	NP_001012745.1:p.Gly241Ala