Canonical Allele Identifier: CA375581247
Gene: AGPAT2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr9:g.139571105T>C (hg19) chr9:g.136676653T>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.136676653T>C , CM000671.2:g.136676653T>C GRCh38
NC_000009.11:g.139571105T>C , CM000671.1:g.139571105T>C GRCh37
NC_000009.10:g.138690926T>C NCBI36
NG_008090.1:g.15807A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000371696.7:c.520A>G MANE Select ENSP00000360761.2:p.Thr174Ala
ENST00000371694.7:c.492+308A>G ENSP00000360759.3:n.492+308A>G
ENST00000371696.6:c.520A>G ENSP00000360761.2:p.Thr174Ala
ENST00000472820.1:n.448A>G
ENST00000538402.1:c.520A>G ENSP00000438919.1:p.Thr174Ala
NM_001012727.1:c.492+308A>G NP_001012745.1:n.492+308A>G
NM_006412.3:c.520A>G NP_006403.2:p.Thr174Ala
NM_006412.4:c.520A>G MANE Select NP_006403.2:p.Thr174Ala
NM_001012727.2:c.492+308A>G NP_001012745.1:n.492+308A>G
Search 100 bp 5'
Search 100 bp 3'