Canonical Allele Identifier: CA591367830

Gene: AGPAT2

Linked Data

• dbSNP Id: rs1475348171
• gnomAD v2: 9-139571370-A-C
• gnomAD v3: 9-136676918-A-C
• gnomAD v4: 9-136676918-A-C
• MyVariant Identifiers: chr9:g.139571370A>C (hg19) ; chr9:g.136676918A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.136676918A>C , CM000671.2:g.136676918A>C	GRCh38
NC_000009.11:g.139571370A>C , CM000671.1:g.139571370A>C	GRCh37
NC_000009.10:g.138691191A>C	NCBI36
NG_008090.1:g.15542T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371696.7:c.492+43T>G MANE Select	ENSP00000360761.2:n.492+43T>G
ENST00000371694.7:c.492+43T>G	ENSP00000360759.3:n.492+43T>G
ENST00000371696.6:c.492+43T>G	ENSP00000360761.2:n.492+43T>G
ENST00000472820.1:n.420+43T>G
ENST00000538402.1:c.492+43T>G	ENSP00000438919.1:n.492+43T>G
NM_001012727.1:c.492+43T>G	NP_001012745.1:n.492+43T>G
NM_006412.3:c.492+43T>G	NP_006403.2:n.492+43T>G
NM_006412.4:c.492+43T>G MANE Select	NP_006403.2:n.492+43T>G
NM_001012727.2:c.492+43T>G	NP_001012745.1:n.492+43T>G