Canonical Allele Identifier: CA375581485
Gene: AGPAT2 HGNC NCBI

Linked Data

dbSNP Id: rs1289409198

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.136676677T>C , CM000671.2:g.136676677T>C GRCh38
NC_000009.11:g.139571129T>C , CM000671.1:g.139571129T>C GRCh37
NC_000009.10:g.138690950T>C NCBI36
NG_008090.1:g.15783A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000371696.7:c.496A>G MANE Select ENSP00000360761.2:p.Lys166Glu
ENST00000371694.7:c.492+284A>G ENSP00000360759.3:n.492+284A>G
ENST00000371696.6:c.496A>G ENSP00000360761.2:p.Lys166Glu
ENST00000472820.1:n.424A>G
ENST00000538402.1:c.496A>G ENSP00000438919.1:p.Lys166Glu
NM_001012727.1:c.492+284A>G NP_001012745.1:n.492+284A>G
NM_006412.3:c.496A>G NP_006403.2:p.Lys166Glu
NM_006412.4:c.496A>G MANE Select NP_006403.2:p.Lys166Glu
NM_001012727.2:c.492+284A>G NP_001012745.1:n.492+284A>G