Canonical Allele Identifier: CA591367907
Gene: AGPAT2 HGNC NCBI

Linked Data

dbSNP Id: rs1187788619
gnomAD v2: 9-139581909-T-G
gnomAD v3: 9-136687457-T-G
gnomAD v4: 9-136687457-T-G
MyVariant Identifiers: chr9:g.139581909T>G (hg19) chr9:g.136687457T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.136687457T>G , CM000671.2:g.136687457T>G GRCh38
NC_000009.11:g.139581909T>G , CM000671.1:g.139581909T>G GRCh37
NC_000009.10:g.138701730T>G NCBI36
NG_008090.1:g.5003A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000371696.7:c.-100A>C MANE Select ENSP00000360761.2:n.-100A>C
NM_001012727.1:c.-100A>C NP_001012745.1:n.-100A>C
NM_006412.3:c.-100A>C NP_006403.2:n.-100A>C
NM_006412.4:c.-100A>C MANE Select NP_006403.2:n.-100A>C
NM_001012727.2:c.-100A>C NP_001012745.1:n.-100A>C
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