Canonical Allele Identifier: CA16042193
Gene: AGPAT2 HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 372111
ClinVar RCV Id: RCV000412578
dbSNP Id: rs1057517655

User contributed link-outs

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.136673913G>A , CM000671.2:g.136673913G>A GRCh38
NC_000009.11:g.139568365G>A , CM000671.1:g.139568365G>A GRCh37
NC_000009.10:g.138688186G>A NCBI36
NG_008090.1:g.18547C>T

Transcript Alleles

HGVS Amino-acid change
NM_001012727.1:c.580C>T VV NP_001012745.1:p.Gln194Ter
NM_006412.3:c.676C>T VV NP_006403.2:p.Gln226Ter
NM_006412.4:c.676C>T VV MANE Preferred NP_006403.2:p.Gln226Ter
ENST00000371694.7:c.580C>T ENSP00000360759.3:p.Gln194Ter
ENST00000371696.6:c.676C>T ENSP00000360761.2:p.Gln226Ter
ENST00000472820.1:n.604C>T
ENST00000538402.1:c.676C>T ENSP00000438919.1:p.Gln226Ter