Canonical Allele Identifier: CA1130033765
Gene: AGPAT2 HGNC NCBI

Linked Data

dbSNP Id: rs1412802600

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.136674817G>C , CM000671.2:g.136674817G>C GRCh38
NC_000009.11:g.139569269G>C , CM000671.1:g.139569269G>C GRCh37
NC_000009.10:g.138689090G>C NCBI36
NG_008090.1:g.17643C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000371696.7:c.589-10C>G MANE Select ENSP00000360761.2:n.589-10C>G
ENST00000371694.7:c.493-10C>G ENSP00000360759.3:n.493-10C>G
ENST00000371696.6:c.589-10C>G ENSP00000360761.2:n.589-10C>G
ENST00000472820.1:n.517-10C>G
ENST00000538402.1:c.589-10C>G ENSP00000438919.1:n.589-10C>G
NM_001012727.1:c.493-10C>G NP_001012745.1:n.493-10C>G
NM_006412.3:c.589-10C>G NP_006403.2:n.589-10C>G
NM_006412.4:c.589-10C>G MANE Select NP_006403.2:n.589-10C>G
NM_001012727.2:c.493-10C>G NP_001012745.1:n.493-10C>G