Canonical Allele Identifier: CA467737180
Gene: AGPAT2 HGNC NCBI

Linked Data

gnomAD v4: 9-136673902-T-C
MyVariant Identifiers: chr9:g.139568354T>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.136673902T>C , CM000671.2:g.136673902T>C GRCh38
NC_000009.11:g.139568354T>C , CM000671.1:g.139568354T>C GRCh37
NC_000009.10:g.138688175T>C NCBI36
NG_008090.1:g.18558A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000371696.7:c.687A>G MANE Select ENSP00000360761.2:p.Glu229=
ENST00000371694.7:c.591A>G ENSP00000360759.3:p.Glu197=
ENST00000371696.6:c.687A>G ENSP00000360761.2:p.Glu229=
ENST00000472820.1:n.615A>G
ENST00000538402.1:c.687A>G ENSP00000438919.1:p.Glu229=
NM_001012727.1:c.591A>G NP_001012745.1:p.Glu197=
NM_006412.3:c.687A>G NP_006403.2:p.Glu229=
NM_006412.4:c.687A>G MANE Select NP_006403.2:p.Glu229=
NM_001012727.2:c.591A>G NP_001012745.1:p.Glu197=
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