Canonical Allele Identifier: CA375580867
Gene: AGPAT2 HGNC NCBI

Linked Data

gnomAD v4: 9-136676605-A-G
MyVariant Identifiers: chr9:g.139571057A>G (hg19) chr9:g.136676605A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.136676605A>G , CM000671.2:g.136676605A>G GRCh38
NC_000009.11:g.139571057A>G , CM000671.1:g.139571057A>G GRCh37
NC_000009.10:g.138690878A>G NCBI36
NG_008090.1:g.15855T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000371696.7:c.568T>C MANE Select ENSP00000360761.2:p.Tyr190His
ENST00000371694.7:c.492+356T>C ENSP00000360759.3:n.492+356T>C
ENST00000371696.6:c.568T>C ENSP00000360761.2:p.Tyr190His
ENST00000472820.1:n.496T>C
ENST00000538402.1:c.568T>C ENSP00000438919.1:p.Tyr190His
NM_001012727.1:c.492+356T>C NP_001012745.1:n.492+356T>C
NM_006412.3:c.568T>C NP_006403.2:p.Tyr190His
NM_006412.4:c.568T>C MANE Select NP_006403.2:p.Tyr190His
NM_001012727.2:c.492+356T>C NP_001012745.1:n.492+356T>C
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