Canonical Allele Identifier: CA861080322
Gene: AGPAT2 HGNC NCBI

Linked Data

dbSNP Id: rs551502234
gnomAD v3: 9-136673536-G-C
gnomAD v4: 9-136673536-G-C
MyVariant Identifiers: chr9:g.139567988G>C (hg19) chr9:g.136673536G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.136673536G>C , CM000671.2:g.136673536G>C GRCh38
NC_000009.11:g.139567988G>C , CM000671.1:g.139567988G>C GRCh37
NC_000009.10:g.138687809G>C NCBI36
NG_008090.1:g.18924C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000371696.7:c.*216C>G MANE Select ENSP00000360761.2:n.*216C>G
ENST00000371694.7:c.*216C>G ENSP00000360759.3:n.*216C>G
ENST00000371696.6:c.*216C>G ENSP00000360761.2:n.*216C>G
ENST00000538402.1:c.*216C>G ENSP00000438919.1:n.*216C>G
NM_001012727.1:c.*216C>G NP_001012745.1:n.*216C>G
NM_006412.3:c.*216C>G NP_006403.2:n.*216C>G
NM_006412.4:c.*216C>G MANE Select NP_006403.2:n.*216C>G
NM_001012727.2:c.*216C>G NP_001012745.1:n.*216C>G
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