Canonical Allele Identifier: CA2692654248
Gene: AGPAT2 HGNC NCBI

Linked Data

gnomAD v4: 9-136674820-A-G
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.136674820A>G , CM000671.2:g.136674820A>G GRCh38
NC_000009.11:g.139569272A>G , CM000671.1:g.139569272A>G GRCh37
NC_000009.10:g.138689093A>G NCBI36
NG_008090.1:g.17640T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000371696.7:c.589-13T>C MANE Select ENSP00000360761.2:n.589-13T>C
ENST00000371694.7:c.493-13T>C ENSP00000360759.3:n.493-13T>C
ENST00000371696.6:c.589-13T>C ENSP00000360761.2:n.589-13T>C
ENST00000472820.1:n.517-13T>C
ENST00000538402.1:c.589-13T>C ENSP00000438919.1:n.589-13T>C
NM_001012727.1:c.493-13T>C NP_001012745.1:n.493-13T>C
NM_006412.3:c.589-13T>C NP_006403.2:n.589-13T>C
NM_006412.4:c.589-13T>C MANE Select NP_006403.2:n.589-13T>C
NM_001012727.2:c.493-13T>C NP_001012745.1:n.493-13T>C
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