Canonical Allele Identifier: CA277949
Gene: AGPAT2 HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 6629
ClinVar RCV Id: RCV000007008
dbSNP Id: rs121908925

User contributed link-outs

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.136674753T>A , CM000671.2:g.136674753T>A GRCh38
NC_000009.10:g.138689026T>A NCBI36
NC_000009.11:g.139569205T>A , CM000671.1:g.139569205T>A GRCh37
NG_008090.1:g.17707A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000371694.7:c.547A>T ENSP00000360759.3:p.Lys183Ter
ENST00000371696.6:c.643A>T ENSP00000360761.2:p.Lys215Ter
ENST00000472820.1:n.571A>T
ENST00000538402.1:c.643A>T ENSP00000438919.1:p.Lys215Ter
NM_001012727.1:c.547A>T VV NP_001012745.1:p.Lys183Ter
NM_006412.3:c.643A>T VV NP_006403.2:p.Lys215Ter