Canonical Allele Identifier: CA5342921

Gene: AGPAT2

Linked Data

• dbSNP Id: rs777267941
• ExAC: 9:139569309 C / T
• gnomAD v2: 9-139569309-C-T
• gnomAD v4: 9-136674857-C-T
• MyVariant Identifiers: chr9:g.139569309C>T (hg19) ; chr9:g.136674857C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.136674857C>T , CM000671.2:g.136674857C>T	GRCh38
NC_000009.11:g.139569309C>T , CM000671.1:g.139569309C>T	GRCh37
NC_000009.10:g.138689130C>T	NCBI36
NG_008090.1:g.17603G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371696.7:c.589-50G>A MANE Select	ENSP00000360761.2:n.589-50G>A
ENST00000371694.7:c.493-50G>A	ENSP00000360759.3:n.493-50G>A
ENST00000371696.6:c.589-50G>A	ENSP00000360761.2:n.589-50G>A
ENST00000472820.1:n.517-50G>A
ENST00000538402.1:c.589-50G>A	ENSP00000438919.1:n.589-50G>A
NM_001012727.1:c.493-50G>A	NP_001012745.1:n.493-50G>A
NM_006412.3:c.589-50G>A	NP_006403.2:n.589-50G>A
NM_006412.4:c.589-50G>A MANE Select	NP_006403.2:n.589-50G>A
NM_001012727.2:c.493-50G>A	NP_001012745.1:n.493-50G>A