Canonical Allele Identifier: CA375580886
Gene: AGPAT2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr9:g.139571059A>C (hg19) chr9:g.136676607A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.136676607A>C , CM000671.2:g.136676607A>C GRCh38
NC_000009.11:g.139571059A>C , CM000671.1:g.139571059A>C GRCh37
NC_000009.10:g.138690880A>C NCBI36
NG_008090.1:g.15853T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000371696.7:c.566T>G MANE Select ENSP00000360761.2:p.Phe189Cys
ENST00000371694.7:c.492+354T>G ENSP00000360759.3:n.492+354T>G
ENST00000371696.6:c.566T>G ENSP00000360761.2:p.Phe189Cys
ENST00000472820.1:n.494T>G
ENST00000538402.1:c.566T>G ENSP00000438919.1:p.Phe189Cys
NM_001012727.1:c.492+354T>G NP_001012745.1:n.492+354T>G
NM_006412.3:c.566T>G NP_006403.2:p.Phe189Cys
NM_006412.4:c.566T>G MANE Select NP_006403.2:p.Phe189Cys
NM_001012727.2:c.492+354T>G NP_001012745.1:n.492+354T>G
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