Canonical Allele Identifier: CA375578618
Gene: AGPAT2 HGNC NCBI

Linked Data

gnomAD v4: 9-136674776-A-G
MyVariant Identifiers: chr9:g.139569228A>G (hg19) chr9:g.136674776A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.136674776A>G , CM000671.2:g.136674776A>G GRCh38
NC_000009.11:g.139569228A>G , CM000671.1:g.139569228A>G GRCh37
NC_000009.10:g.138689049A>G NCBI36
NG_008090.1:g.17684T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000371696.7:c.620T>C MANE Select ENSP00000360761.2:p.Phe207Ser
ENST00000371694.7:c.524T>C ENSP00000360759.3:p.Phe175Ser
ENST00000371696.6:c.620T>C ENSP00000360761.2:p.Phe207Ser
ENST00000472820.1:n.548T>C
ENST00000538402.1:c.620T>C ENSP00000438919.1:p.Phe207Ser
NM_001012727.1:c.524T>C NP_001012745.1:p.Phe175Ser
NM_006412.3:c.620T>C NP_006403.2:p.Phe207Ser
NM_006412.4:c.620T>C MANE Select NP_006403.2:p.Phe207Ser
NM_001012727.2:c.524T>C NP_001012745.1:p.Phe175Ser
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