Canonical Allele Identifier: CA1130033030
Gene: AGPAT2 HGNC NCBI

Linked Data

dbSNP Id: rs1846043698
gnomAD v3: 9-136673743-T-C
gnomAD v4: 9-136673743-T-C
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.136673743T>C , CM000671.2:g.136673743T>C GRCh38
NC_000009.11:g.139568195T>C , CM000671.1:g.139568195T>C GRCh37
NC_000009.10:g.138688016T>C NCBI36
NG_008090.1:g.18717A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000371696.7:c.*9A>G MANE Select ENSP00000360761.2:n.*9A>G
ENST00000371694.7:c.*9A>G ENSP00000360759.3:n.*9A>G
ENST00000371696.6:c.*9A>G ENSP00000360761.2:n.*9A>G
ENST00000472820.1:n.774A>G
ENST00000538402.1:c.*9A>G ENSP00000438919.1:n.*9A>G
NM_001012727.1:c.*9A>G NP_001012745.1:n.*9A>G
NM_006412.3:c.*9A>G NP_006403.2:n.*9A>G
NM_006412.4:c.*9A>G MANE Select NP_006403.2:n.*9A>G
NM_001012727.2:c.*9A>G NP_001012745.1:n.*9A>G
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