Canonical Allele Identifier: CA467737135
Gene: AGPAT2 HGNC NCBI

Linked Data

gnomAD v4: 9-136673878-A-T
MyVariant Identifiers: chr9:g.139568330A>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.136673878A>T , CM000671.2:g.136673878A>T GRCh38
NC_000009.11:g.139568330A>T , CM000671.1:g.139568330A>T GRCh37
NC_000009.10:g.138688151A>T NCBI36
NG_008090.1:g.18582T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000371696.7:c.711T>A MANE Select ENSP00000360761.2:p.Thr237=
ENST00000371694.7:c.615T>A ENSP00000360759.3:p.Thr205=
ENST00000371696.6:c.711T>A ENSP00000360761.2:p.Thr237=
ENST00000472820.1:n.639T>A
ENST00000538402.1:c.711T>A ENSP00000438919.1:p.Thr237=
NM_001012727.1:c.615T>A NP_001012745.1:p.Thr205=
NM_006412.3:c.711T>A NP_006403.2:p.Thr237=
NM_006412.4:c.711T>A MANE Select NP_006403.2:p.Thr237=
NM_001012727.2:c.615T>A NP_001012745.1:p.Thr205=
Search 100 bp 5'
Search 100 bp 3'