Canonical Allele Identifier: CA375588027
Gene: AGPAT2 HGNC NCBI

Linked Data

dbSNP Id: rs1213688450
gnomAD v2: 9-139581685-G-A
gnomAD v3: 9-136687233-G-A
gnomAD v4: 9-136687233-G-A
MyVariant Identifiers: chr9:g.139581685G>A (hg19) chr9:g.136687233G>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.136687233G>A , CM000671.2:g.136687233G>A GRCh38
NC_000009.11:g.139581685G>A , CM000671.1:g.139581685G>A GRCh37
NC_000009.10:g.138701506G>A NCBI36
NG_008090.1:g.5227C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000371696.7:c.125C>T MANE Select ENSP00000360761.2:p.Ala42Val
ENST00000371694.7:c.125C>T ENSP00000360759.3:p.Ala42Val
ENST00000371696.6:c.125C>T ENSP00000360761.2:p.Ala42Val
ENST00000470861.1:n.133C>T
ENST00000538402.1:c.125C>T ENSP00000438919.1:p.Ala42Val
NM_001012727.1:c.125C>T NP_001012745.1:p.Ala42Val
NM_006412.3:c.125C>T NP_006403.2:p.Ala42Val
NM_006412.4:c.125C>T MANE Select NP_006403.2:p.Ala42Val
NM_001012727.2:c.125C>T NP_001012745.1:p.Ala42Val
Search 100 bp 5'
Search 100 bp 3'