Canonical Allele Identifier: CA201623200
Gene: AGPAT2 HGNC NCBI

Linked Data

ClinVar Variation Id: 914525
ClinVar RCV Id: RCV001168727
dbSNP Id: rs182766891
gnomAD v2: 9-139567993-C-T
gnomAD v3: 9-136673541-C-T
gnomAD v4: 9-136673541-C-T
MyVariant Identifiers: chr9:g.139567993C>T (hg19) chr9:g.136673541C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.136673541C>T , CM000671.2:g.136673541C>T GRCh38
NC_000009.11:g.139567993C>T , CM000671.1:g.139567993C>T GRCh37
NC_000009.10:g.138687814C>T NCBI36
NG_008090.1:g.18919G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000371696.7:c.*211G>A MANE Select ENSP00000360761.2:n.*211G>A
ENST00000371694.7:c.*211G>A ENSP00000360759.3:n.*211G>A
ENST00000371696.6:c.*211G>A ENSP00000360761.2:n.*211G>A
ENST00000538402.1:c.*211G>A ENSP00000438919.1:n.*211G>A
NM_001012727.1:c.*211G>A NP_001012745.1:n.*211G>A
NM_006412.3:c.*211G>A NP_006403.2:n.*211G>A
NM_006412.4:c.*211G>A MANE Select NP_006403.2:n.*211G>A
NM_001012727.2:c.*211G>A NP_001012745.1:n.*211G>A
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