Canonical Allele Identifier: CA375588080
Gene: AGPAT2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr9:g.139581697A>C (hg19) chr9:g.136687245A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.136687245A>C , CM000671.2:g.136687245A>C GRCh38
NC_000009.11:g.139581697A>C , CM000671.1:g.139581697A>C GRCh37
NC_000009.10:g.138701518A>C NCBI36
NG_008090.1:g.5215T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000371696.7:c.113T>G MANE Select ENSP00000360761.2:p.Phe38Cys
ENST00000371694.7:c.113T>G ENSP00000360759.3:p.Phe38Cys
ENST00000371696.6:c.113T>G ENSP00000360761.2:p.Phe38Cys
ENST00000470861.1:n.121T>G
ENST00000538402.1:c.113T>G ENSP00000438919.1:p.Phe38Cys
NM_001012727.1:c.113T>G NP_001012745.1:p.Phe38Cys
NM_006412.3:c.113T>G NP_006403.2:p.Phe38Cys
NM_006412.4:c.113T>G MANE Select NP_006403.2:p.Phe38Cys
NM_001012727.2:c.113T>G NP_001012745.1:p.Phe38Cys
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