Canonical Allele Identifier: CA467744308
Gene: AGPAT2 HGNC NCBI

Linked Data

gnomAD v4: 9-136687334-G-T
MyVariant Identifiers: chr9:g.139581786G>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.136687334G>T , CM000671.2:g.136687334G>T GRCh38
NC_000009.11:g.139581786G>T , CM000671.1:g.139581786G>T GRCh37
NC_000009.10:g.138701607G>T NCBI36
NG_008090.1:g.5126C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000371696.7:c.24C>A MANE Select ENSP00000360761.2:p.Ala8=
ENST00000371694.7:c.24C>A ENSP00000360759.3:p.Ala8=
ENST00000371696.6:c.24C>A ENSP00000360761.2:p.Ala8=
ENST00000470861.1:n.32C>A
ENST00000538402.1:c.24C>A ENSP00000438919.1:p.Ala8=
NM_001012727.1:c.24C>A NP_001012745.1:p.Ala8=
NM_006412.3:c.24C>A NP_006403.2:p.Ala8=
NM_006412.4:c.24C>A MANE Select NP_006403.2:p.Ala8=
NM_001012727.2:c.24C>A NP_001012745.1:p.Ala8=
Search 100 bp 5'
Search 100 bp 3'