Canonical Allele Identifier: CA375577795
Gene: AGPAT2 HGNC NCBI

Linked Data

dbSNP Id: rs1846049961

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.136673924G>A , CM000671.2:g.136673924G>A GRCh38
NC_000009.11:g.139568376G>A , CM000671.1:g.139568376G>A GRCh37
NC_000009.10:g.138688197G>A NCBI36
NG_008090.1:g.18536C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000371696.7:c.665C>T MANE Select ENSP00000360761.2:p.Thr222Ile
ENST00000371694.7:c.569C>T ENSP00000360759.3:p.Thr190Ile
ENST00000371696.6:c.665C>T ENSP00000360761.2:p.Thr222Ile
ENST00000472820.1:n.593C>T
ENST00000538402.1:c.665C>T ENSP00000438919.1:p.Thr222Ile
NM_001012727.1:c.569C>T NP_001012745.1:p.Thr190Ile
NM_006412.3:c.665C>T NP_006403.2:p.Thr222Ile
NM_006412.4:c.665C>T MANE Select NP_006403.2:p.Thr222Ile
NM_001012727.2:c.569C>T NP_001012745.1:p.Thr190Ile