Canonical Allele Identifier: CA467744069
Gene: AGPAT2 HGNC NCBI

Linked Data

dbSNP Id: rs1332119400
gnomAD v2: 9-139581726-G-A
gnomAD v3: 9-136687274-G-A
gnomAD v4: 9-136687274-G-A
MyVariant Identifiers: chr9:g.139581726G>A (hg19) chr9:g.136687274G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.136687274G>A , CM000671.2:g.136687274G>A GRCh38
NC_000009.11:g.139581726G>A , CM000671.1:g.139581726G>A GRCh37
NC_000009.10:g.138701547G>A NCBI36
NG_008090.1:g.5186C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000371696.7:c.84C>T MANE Select ENSP00000360761.2:p.Ala28=
ENST00000371694.7:c.84C>T ENSP00000360759.3:p.Ala28=
ENST00000371696.6:c.84C>T ENSP00000360761.2:p.Ala28=
ENST00000470861.1:n.92C>T
ENST00000538402.1:c.84C>T ENSP00000438919.1:p.Ala28=
NM_001012727.1:c.84C>T NP_001012745.1:p.Ala28=
NM_006412.3:c.84C>T NP_006403.2:p.Ala28=
NM_006412.4:c.84C>T MANE Select NP_006403.2:p.Ala28=
NM_001012727.2:c.84C>T NP_001012745.1:p.Ala28=
Search 100 bp 5'
Search 100 bp 3'