Canonical Allele Identifier: CA375578593
Gene: AGPAT2 HGNC NCBI

Linked Data

gnomAD v4: 9-136674771-A-G
MyVariant Identifiers: chr9:g.139569223A>G (hg19) chr9:g.136674771A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.136674771A>G , CM000671.2:g.136674771A>G GRCh38
NC_000009.11:g.139569223A>G , CM000671.1:g.139569223A>G GRCh37
NC_000009.10:g.138689044A>G NCBI36
NG_008090.1:g.17689T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000371696.7:c.625T>C MANE Select ENSP00000360761.2:p.Ser209Pro
ENST00000371694.7:c.529T>C ENSP00000360759.3:p.Ser177Pro
ENST00000371696.6:c.625T>C ENSP00000360761.2:p.Ser209Pro
ENST00000472820.1:n.553T>C
ENST00000538402.1:c.625T>C ENSP00000438919.1:p.Ser209Pro
NM_001012727.1:c.529T>C NP_001012745.1:p.Ser177Pro
NM_006412.3:c.625T>C NP_006403.2:p.Ser209Pro
NM_006412.4:c.625T>C MANE Select NP_006403.2:p.Ser209Pro
NM_001012727.2:c.529T>C NP_001012745.1:p.Ser177Pro
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