Canonical Allele Identifier: CA861082077

Gene: AGPAT2

Linked Data

• dbSNP Id: rs1166411216
• gnomAD v3: 9-136676104-C-T
• gnomAD v4: 9-136676104-C-T
• MyVariant Identifiers: chr9:g.139570556C>T (hg19) ; chr9:g.136676104C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.136676104C>T , CM000671.2:g.136676104C>T	GRCh38
NC_000009.11:g.139570556C>T , CM000671.1:g.139570556C>T	GRCh37
NC_000009.10:g.138690377C>T	NCBI36
NG_008090.1:g.16356G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000371696.7:c.588+481G>A MANE Select	ENSP00000360761.2:n.588+481G>A
ENST00000371694.7:c.492+857G>A	ENSP00000360759.3:n.492+857G>A
ENST00000371696.6:c.588+481G>A	ENSP00000360761.2:n.588+481G>A
ENST00000472820.1:n.516+481G>A
ENST00000538402.1:c.588+481G>A	ENSP00000438919.1:n.588+481G>A
NM_001012727.1:c.492+857G>A	NP_001012745.1:n.492+857G>A
NM_006412.3:c.588+481G>A	NP_006403.2:n.588+481G>A
NM_006412.4:c.588+481G>A MANE Select	NP_006403.2:n.588+481G>A
NM_001012727.2:c.492+857G>A	NP_001012745.1:n.492+857G>A