Canonical Allele Identifier: CA467738171
Gene: AGPAT2 HGNC NCBI

Linked Data

gnomAD v4: 9-136674769-G-C
MyVariant Identifiers: chr9:g.139569221G>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.136674769G>C , CM000671.2:g.136674769G>C GRCh38
NC_000009.11:g.139569221G>C , CM000671.1:g.139569221G>C GRCh37
NC_000009.10:g.138689042G>C NCBI36
NG_008090.1:g.17691C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000371696.7:c.627C>G MANE Select ENSP00000360761.2:p.Ser209=
ENST00000371694.7:c.531C>G ENSP00000360759.3:p.Ser177=
ENST00000371696.6:c.627C>G ENSP00000360761.2:p.Ser209=
ENST00000472820.1:n.555C>G
ENST00000538402.1:c.627C>G ENSP00000438919.1:p.Ser209=
NM_001012727.1:c.531C>G NP_001012745.1:p.Ser177=
NM_006412.3:c.627C>G NP_006403.2:p.Ser209=
NM_006412.4:c.627C>G MANE Select NP_006403.2:p.Ser209=
NM_001012727.2:c.531C>G NP_001012745.1:p.Ser177=
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