Canonical Allele Identifier: CA16042199
Gene: AGPAT2 HGNC NCBI

Linked Data

ClinVar Variation Id: 372103
ClinVar RCV Id: RCV000412655
dbSNP Id: rs1057517650

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.136687175C>T , CM000671.2:g.136687175C>T GRCh38
NC_000009.11:g.139581627C>T , CM000671.1:g.139581627C>T GRCh37
NC_000009.10:g.138701448C>T NCBI36
NG_008090.1:g.5285G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000371696.7:c.182+1G>A MANE Select ENSP00000360761.2:n.182+1G>A
ENST00000371694.7:c.182+1G>A ENSP00000360759.3:n.182+1G>A
ENST00000371696.6:c.182+1G>A ENSP00000360761.2:n.182+1G>A
ENST00000470861.1:n.190+1G>A
ENST00000538402.1:c.182+1G>A ENSP00000438919.1:n.182+1G>A
NM_001012727.1:c.182+1G>A NP_001012745.1:n.182+1G>A
NM_006412.3:c.182+1G>A NP_006403.2:n.182+1G>A
NM_006412.4:c.182+1G>A MANE Select NP_006403.2:n.182+1G>A
NM_001012727.2:c.182+1G>A NP_001012745.1:n.182+1G>A