Canonical Allele Identifier: CA467744138
Gene: AGPAT2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr9:g.139581738G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.136687286G>A , CM000671.2:g.136687286G>A GRCh38
NC_000009.11:g.139581738G>A , CM000671.1:g.139581738G>A GRCh37
NC_000009.10:g.138701559G>A NCBI36
NG_008090.1:g.5174C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000371696.7:c.72C>T MANE Select ENSP00000360761.2:p.Ala24=
ENST00000371694.7:c.72C>T ENSP00000360759.3:p.Ala24=
ENST00000371696.6:c.72C>T ENSP00000360761.2:p.Ala24=
ENST00000470861.1:n.80C>T
ENST00000538402.1:c.72C>T ENSP00000438919.1:p.Ala24=
NM_001012727.1:c.72C>T NP_001012745.1:p.Ala24=
NM_006412.3:c.72C>T NP_006403.2:p.Ala24=
NM_006412.4:c.72C>T MANE Select NP_006403.2:p.Ala24=
NM_001012727.2:c.72C>T NP_001012745.1:p.Ala24=