Canonical Allele Identifier: CA467738256
Gene: AGPAT2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr9:g.139569233A>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.136674781A>G , CM000671.2:g.136674781A>G GRCh38
NC_000009.11:g.139569233A>G , CM000671.1:g.139569233A>G GRCh37
NC_000009.10:g.138689054A>G NCBI36
NG_008090.1:g.17679T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000371696.7:c.615T>C MANE Select ENSP00000360761.2:p.Ser205=
ENST00000371694.7:c.519T>C ENSP00000360759.3:p.Ser173=
ENST00000371696.6:c.615T>C ENSP00000360761.2:p.Ser205=
ENST00000472820.1:n.543T>C
ENST00000538402.1:c.615T>C ENSP00000438919.1:p.Ser205=
NM_001012727.1:c.519T>C NP_001012745.1:p.Ser173=
NM_006412.3:c.615T>C NP_006403.2:p.Ser205=
NM_006412.4:c.615T>C MANE Select NP_006403.2:p.Ser205=
NM_001012727.2:c.519T>C NP_001012745.1:p.Ser173=