Canonical Allele Identifier: CA1130033712
Gene: AGPAT2 HGNC NCBI

Linked Data

dbSNP Id: rs1846067187
gnomAD v3: 9-136674716-T-C
gnomAD v4: 9-136674716-T-C
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.136674716T>C , CM000671.2:g.136674716T>C GRCh38
NC_000009.11:g.139569168T>C , CM000671.1:g.139569168T>C GRCh37
NC_000009.10:g.138688989T>C NCBI36
NG_008090.1:g.17744A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000371696.7:c.661+19A>G MANE Select ENSP00000360761.2:n.661+19A>G
ENST00000371694.7:c.565+19A>G ENSP00000360759.3:n.565+19A>G
ENST00000371696.6:c.661+19A>G ENSP00000360761.2:n.661+19A>G
ENST00000472820.1:n.589+19A>G
ENST00000538402.1:c.661+19A>G ENSP00000438919.1:n.661+19A>G
NM_001012727.1:c.565+19A>G NP_001012745.1:n.565+19A>G
NM_006412.3:c.661+19A>G NP_006403.2:n.661+19A>G
NM_006412.4:c.661+19A>G MANE Select NP_006403.2:n.661+19A>G
NM_001012727.2:c.565+19A>G NP_001012745.1:n.565+19A>G
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