Canonical Allele Identifier: CA375588129
Gene: AGPAT2 HGNC NCBI

Linked Data

dbSNP Id: rs1460980367
gnomAD v2: 9-139581710-A-C
MyVariant Identifiers: chr9:g.139581710A>C (hg19) chr9:g.136687258A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.136687258A>C , CM000671.2:g.136687258A>C GRCh38
NC_000009.11:g.139581710A>C , CM000671.1:g.139581710A>C GRCh37
NC_000009.10:g.138701531A>C NCBI36
NG_008090.1:g.5202T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000371696.7:c.100T>G MANE Select ENSP00000360761.2:p.Cys34Gly
ENST00000371694.7:c.100T>G ENSP00000360759.3:p.Cys34Gly
ENST00000371696.6:c.100T>G ENSP00000360761.2:p.Cys34Gly
ENST00000470861.1:n.108T>G
ENST00000538402.1:c.100T>G ENSP00000438919.1:p.Cys34Gly
NM_001012727.1:c.100T>G NP_001012745.1:p.Cys34Gly
NM_006412.3:c.100T>G NP_006403.2:p.Cys34Gly
NM_006412.4:c.100T>G MANE Select NP_006403.2:p.Cys34Gly
NM_001012727.2:c.100T>G NP_001012745.1:p.Cys34Gly
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