Canonical Allele Identifier: CA375588244
Gene: AGPAT2 HGNC NCBI

Linked Data

gnomAD v3: 9-136687282-A-T
gnomAD v4: 9-136687282-A-T
MyVariant Identifiers: chr9:g.139581734A>T (hg19) chr9:g.136687282A>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.136687282A>T , CM000671.2:g.136687282A>T GRCh38
NC_000009.11:g.139581734A>T , CM000671.1:g.139581734A>T GRCh37
NC_000009.10:g.138701555A>T NCBI36
NG_008090.1:g.5178T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000371696.7:c.76T>A MANE Select ENSP00000360761.2:p.Phe26Ile
ENST00000371694.7:c.76T>A ENSP00000360759.3:p.Phe26Ile
ENST00000371696.6:c.76T>A ENSP00000360761.2:p.Phe26Ile
ENST00000470861.1:n.84T>A
ENST00000538402.1:c.76T>A ENSP00000438919.1:p.Phe26Ile
NM_001012727.1:c.76T>A NP_001012745.1:p.Phe26Ile
NM_006412.3:c.76T>A NP_006403.2:p.Phe26Ile
NM_006412.4:c.76T>A MANE Select NP_006403.2:p.Phe26Ile
NM_001012727.2:c.76T>A NP_001012745.1:p.Phe26Ile
Search 100 bp 5'
Search 100 bp 3'