Canonical Allele Identifier: CA375578166
Gene: AGPAT2 HGNC NCBI

Linked Data

dbSNP Id: rs1237838088

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.136674741T>C , CM000671.2:g.136674741T>C GRCh38
NC_000009.11:g.139569193T>C , CM000671.1:g.139569193T>C GRCh37
NC_000009.10:g.138689014T>C NCBI36
NG_008090.1:g.17719A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000371696.7:c.655A>G MANE Select ENSP00000360761.2:p.Thr219Ala
ENST00000371694.7:c.559A>G ENSP00000360759.3:p.Thr187Ala
ENST00000371696.6:c.655A>G ENSP00000360761.2:p.Thr219Ala
ENST00000472820.1:n.583A>G
ENST00000538402.1:c.655A>G ENSP00000438919.1:p.Thr219Ala
NM_001012727.1:c.559A>G NP_001012745.1:p.Thr187Ala
NM_006412.3:c.655A>G NP_006403.2:p.Thr219Ala
NM_006412.4:c.655A>G MANE Select NP_006403.2:p.Thr219Ala
NM_001012727.2:c.559A>G NP_001012745.1:p.Thr187Ala