Canonical Allele Identifier: CA201641451
Gene: AGPAT2 HGNC NCBI

Linked Data

dbSNP Id: rs1012305332
gnomAD v2: 9-139581719-C-A
gnomAD v3: 9-136687267-C-A
gnomAD v4: 9-136687267-C-A
MyVariant Identifiers: chr9:g.139581719C>A (hg19) chr9:g.136687267C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.136687267C>A , CM000671.2:g.136687267C>A GRCh38
NC_000009.11:g.139581719C>A , CM000671.1:g.139581719C>A GRCh37
NC_000009.10:g.138701540C>A NCBI36
NG_008090.1:g.5193G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000371696.7:c.91G>T MANE Select ENSP00000360761.2:p.Ala31Ser
ENST00000371694.7:c.91G>T ENSP00000360759.3:p.Ala31Ser
ENST00000371696.6:c.91G>T ENSP00000360761.2:p.Ala31Ser
ENST00000470861.1:n.99G>T
ENST00000538402.1:c.91G>T ENSP00000438919.1:p.Ala31Ser
NM_001012727.1:c.91G>T NP_001012745.1:p.Ala31Ser
NM_006412.3:c.91G>T NP_006403.2:p.Ala31Ser
NM_006412.4:c.91G>T MANE Select NP_006403.2:p.Ala31Ser
NM_001012727.2:c.91G>T NP_001012745.1:p.Ala31Ser
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