Canonical Allele Identifier: CA277944
Gene: AGPAT2 HGNC NCBI

Linked Data

ClinVar Variation Id: 6625
dbSNP Id: rs116807569

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.136674809T>C , CM000671.2:g.136674809T>C GRCh38
NC_000009.11:g.139569261T>C , CM000671.1:g.139569261T>C GRCh37
NC_000009.10:g.138689082T>C NCBI36
NG_008090.1:g.17651A>G

Transcript Alleles

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