Canonical Allele Identifier: CA2720764859
Gene: AGPAT2 HGNC NCBI

Linked Data

dbSNP Id: rs566363731
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.136674681G>C , CM000671.2:g.136674681G>C GRCh38
NC_000009.11:g.139569133G>C , CM000671.1:g.139569133G>C GRCh37
NC_000009.10:g.138688954G>C NCBI36
NG_008090.1:g.17779C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000371696.7:c.661+54C>G MANE Select ENSP00000360761.2:n.661+54C>G
ENST00000371694.7:c.565+54C>G ENSP00000360759.3:n.565+54C>G
ENST00000371696.6:c.661+54C>G ENSP00000360761.2:n.661+54C>G
ENST00000472820.1:n.589+54C>G
ENST00000538402.1:c.661+54C>G ENSP00000438919.1:n.661+54C>G
NM_001012727.1:c.565+54C>G NP_001012745.1:n.565+54C>G
NM_006412.3:c.661+54C>G NP_006403.2:n.661+54C>G
NM_006412.4:c.661+54C>G MANE Select NP_006403.2:n.661+54C>G
NM_001012727.2:c.565+54C>G NP_001012745.1:n.565+54C>G
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