Canonical Allele Identifier: CA201623258
Gene: AGPAT2 HGNC NCBI

Linked Data

dbSNP Id: rs886913580
gnomAD v3: 9-136673593-A-G
gnomAD v4: 9-136673593-A-G
MyVariant Identifiers: chr9:g.139568045A>G (hg19) chr9:g.136673593A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.136673593A>G , CM000671.2:g.136673593A>G GRCh38
NC_000009.11:g.139568045A>G , CM000671.1:g.139568045A>G GRCh37
NC_000009.10:g.138687866A>G NCBI36
NG_008090.1:g.18867T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000371696.7:c.*159T>C MANE Select ENSP00000360761.2:n.*159T>C
ENST00000371694.7:c.*159T>C ENSP00000360759.3:n.*159T>C
ENST00000371696.6:c.*159T>C ENSP00000360761.2:n.*159T>C
ENST00000538402.1:c.*159T>C ENSP00000438919.1:n.*159T>C
NM_001012727.1:c.*159T>C NP_001012745.1:n.*159T>C
NM_006412.3:c.*159T>C NP_006403.2:n.*159T>C
NM_006412.4:c.*159T>C MANE Select NP_006403.2:n.*159T>C
NM_001012727.2:c.*159T>C NP_001012745.1:n.*159T>C
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