Canonical Allele Identifier: CA467743655
Gene: AGPAT2 HGNC NCBI

Linked Data

dbSNP Id: rs1480049326

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.136687181G>A , CM000671.2:g.136687181G>A GRCh38
NC_000009.11:g.139581633G>A , CM000671.1:g.139581633G>A GRCh37
NC_000009.10:g.138701454G>A NCBI36
NG_008090.1:g.5279C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000371696.7:c.177C>T MANE Select ENSP00000360761.2:p.Asn59=
ENST00000371694.7:c.177C>T ENSP00000360759.3:p.Asn59=
ENST00000371696.6:c.177C>T ENSP00000360761.2:p.Asn59=
ENST00000470861.1:n.185C>T
ENST00000538402.1:c.177C>T ENSP00000438919.1:p.Asn59=
NM_001012727.1:c.177C>T NP_001012745.1:p.Asn59=
NM_006412.3:c.177C>T NP_006403.2:p.Asn59=
NM_006412.4:c.177C>T MANE Select NP_006403.2:p.Asn59=
NM_001012727.2:c.177C>T NP_001012745.1:p.Asn59=