Canonical Allele Identifier: CA467743790
Gene: AGPAT2 HGNC NCBI

Linked Data

gnomAD v4: 9-136687226-G-A
MyVariant Identifiers: chr9:g.139581678G>A (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.136687226G>A , CM000671.2:g.136687226G>A GRCh38
NC_000009.11:g.139581678G>A , CM000671.1:g.139581678G>A GRCh37
NC_000009.10:g.138701499G>A NCBI36
NG_008090.1:g.5234C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000371696.7:c.132C>T MANE Select ENSP00000360761.2:p.Ala44=
ENST00000371694.7:c.132C>T ENSP00000360759.3:p.Ala44=
ENST00000371696.6:c.132C>T ENSP00000360761.2:p.Ala44=
ENST00000470861.1:n.140C>T
ENST00000538402.1:c.132C>T ENSP00000438919.1:p.Ala44=
NM_001012727.1:c.132C>T NP_001012745.1:p.Ala44=
NM_006412.3:c.132C>T NP_006403.2:p.Ala44=
NM_006412.4:c.132C>T MANE Select NP_006403.2:p.Ala44=
NM_001012727.2:c.132C>T NP_001012745.1:p.Ala44=
Search 100 bp 5'
Search 100 bp 3'