Canonical Allele Identifier: CA375578980
Gene: AGPAT2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr9:g.139569258A>C (hg19) chr9:g.136674806A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.136674806A>C , CM000671.2:g.136674806A>C GRCh38
NC_000009.11:g.139569258A>C , CM000671.1:g.139569258A>C GRCh37
NC_000009.10:g.138689079A>C NCBI36
NG_008090.1:g.17654T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000371696.7:c.590T>G MANE Select ENSP00000360761.2:p.Val197Gly
ENST00000371694.7:c.494T>G ENSP00000360759.3:p.Val165Gly
ENST00000371696.6:c.590T>G ENSP00000360761.2:p.Val197Gly
ENST00000472820.1:n.518T>G
ENST00000538402.1:c.590T>G ENSP00000438919.1:p.Val197Gly
NM_001012727.1:c.494T>G NP_001012745.1:p.Val165Gly
NM_006412.3:c.590T>G NP_006403.2:p.Val197Gly
NM_006412.4:c.590T>G MANE Select NP_006403.2:p.Val197Gly
NM_001012727.2:c.494T>G NP_001012745.1:p.Val165Gly
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