Canonical Allele Identifier: CA591367903
Gene: AGPAT2 HGNC NCBI

Linked Data

dbSNP Id: rs1311221138
gnomAD v2: 9-139581891-T-A
gnomAD v3: 9-136687439-T-A
gnomAD v4: 9-136687439-T-A
MyVariant Identifiers: chr9:g.139581891T>A (hg19) chr9:g.136687439T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.136687439T>A , CM000671.2:g.136687439T>A GRCh38
NC_000009.11:g.139581891T>A , CM000671.1:g.139581891T>A GRCh37
NC_000009.10:g.138701712T>A NCBI36
NG_008090.1:g.5021A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000371696.7:c.-82A>T MANE Select ENSP00000360761.2:n.-82A>T
NM_001012727.1:c.-82A>T NP_001012745.1:n.-82A>T
NM_006412.3:c.-82A>T NP_006403.2:n.-82A>T
NM_006412.4:c.-82A>T MANE Select NP_006403.2:n.-82A>T
NM_001012727.2:c.-82A>T NP_001012745.1:n.-82A>T
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