Canonical Allele Identifier: CA375580862
Gene: AGPAT2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr9:g.139571056T>C (hg19) chr9:g.136676604T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.136676604T>C , CM000671.2:g.136676604T>C GRCh38
NC_000009.11:g.139571056T>C , CM000671.1:g.139571056T>C GRCh37
NC_000009.10:g.138690877T>C NCBI36
NG_008090.1:g.15856A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000371696.7:c.569A>G MANE Select ENSP00000360761.2:p.Tyr190Cys
ENST00000371694.7:c.492+357A>G ENSP00000360759.3:n.492+357A>G
ENST00000371696.6:c.569A>G ENSP00000360761.2:p.Tyr190Cys
ENST00000472820.1:n.497A>G
ENST00000538402.1:c.569A>G ENSP00000438919.1:p.Tyr190Cys
NM_001012727.1:c.492+357A>G NP_001012745.1:n.492+357A>G
NM_006412.3:c.569A>G NP_006403.2:p.Tyr190Cys
NM_006412.4:c.569A>G MANE Select NP_006403.2:p.Tyr190Cys
NM_001012727.2:c.492+357A>G NP_001012745.1:n.492+357A>G
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