Canonical Allele Identifier: CA375587884
Gene: AGPAT2 HGNC NCBI

Linked Data

gnomAD v4: 9-136687192-T-C
MyVariant Identifiers: chr9:g.139581644T>C (hg19) chr9:g.136687192T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.136687192T>C , CM000671.2:g.136687192T>C GRCh38
NC_000009.11:g.139581644T>C , CM000671.1:g.139581644T>C GRCh37
NC_000009.10:g.138701465T>C NCBI36
NG_008090.1:g.5268A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000371696.7:c.166A>G MANE Select ENSP00000360761.2:p.Thr56Ala
ENST00000371694.7:c.166A>G ENSP00000360759.3:p.Thr56Ala
ENST00000371696.6:c.166A>G ENSP00000360761.2:p.Thr56Ala
ENST00000470861.1:n.174A>G
ENST00000538402.1:c.166A>G ENSP00000438919.1:p.Thr56Ala
NM_001012727.1:c.166A>G NP_001012745.1:p.Thr56Ala
NM_006412.3:c.166A>G NP_006403.2:p.Thr56Ala
NM_006412.4:c.166A>G MANE Select NP_006403.2:p.Thr56Ala
NM_001012727.2:c.166A>G NP_001012745.1:p.Thr56Ala
Search 100 bp 5'
Search 100 bp 3'