Canonical Allele Identifier: CA375587850
Gene: AGPAT2 HGNC NCBI

Linked Data

dbSNP Id: rs1846233178

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.136687183T>G , CM000671.2:g.136687183T>G GRCh38
NC_000009.11:g.139581635T>G , CM000671.1:g.139581635T>G GRCh37
NC_000009.10:g.138701456T>G NCBI36
NG_008090.1:g.5277A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000371696.7:c.175A>C MANE Select ENSP00000360761.2:p.Asn59His
ENST00000371694.7:c.175A>C ENSP00000360759.3:p.Asn59His
ENST00000371696.6:c.175A>C ENSP00000360761.2:p.Asn59His
ENST00000470861.1:n.183A>C
ENST00000538402.1:c.175A>C ENSP00000438919.1:p.Asn59His
NM_001012727.1:c.175A>C NP_001012745.1:p.Asn59His
NM_006412.3:c.175A>C NP_006403.2:p.Asn59His
NM_006412.4:c.175A>C MANE Select NP_006403.2:p.Asn59His
NM_001012727.2:c.175A>C NP_001012745.1:p.Asn59His