Canonical Allele Identifier: CA467738757
Gene: AGPAT2 HGNC NCBI

Linked Data

dbSNP Id: rs756686507
gnomAD v3: 9-136676612-G-T
gnomAD v4: 9-136676612-G-T
MyVariant Identifiers: chr9:g.139571064G>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.136676612G>T , CM000671.2:g.136676612G>T GRCh38
NC_000009.11:g.139571064G>T , CM000671.1:g.139571064G>T GRCh37
NC_000009.10:g.138690885G>T NCBI36
NG_008090.1:g.15848C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000371696.7:c.561C>A MANE Select ENSP00000360761.2:p.Gly187=
ENST00000371694.7:c.492+349C>A ENSP00000360759.3:n.492+349C>A
ENST00000371696.6:c.561C>A ENSP00000360761.2:p.Gly187=
ENST00000472820.1:n.489C>A
ENST00000538402.1:c.561C>A ENSP00000438919.1:p.Gly187=
NM_001012727.1:c.492+349C>A NP_001012745.1:n.492+349C>A
NM_006412.3:c.561C>A NP_006403.2:p.Gly187=
NM_006412.4:c.561C>A MANE Select NP_006403.2:p.Gly187=
NM_001012727.2:c.492+349C>A NP_001012745.1:n.492+349C>A
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