Canonical Allele Identifier: CA467738295
Gene: AGPAT2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr9:g.139569242C>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.136674790C>A , CM000671.2:g.136674790C>A GRCh38
NC_000009.11:g.139569242C>A , CM000671.1:g.139569242C>A GRCh37
NC_000009.10:g.138689063C>A NCBI36
NG_008090.1:g.17670G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000371696.7:c.606G>T MANE Select ENSP00000360761.2:p.Val202=
ENST00000371694.7:c.510G>T ENSP00000360759.3:p.Val170=
ENST00000371696.6:c.606G>T ENSP00000360761.2:p.Val202=
ENST00000472820.1:n.534G>T
ENST00000538402.1:c.606G>T ENSP00000438919.1:p.Val202=
NM_001012727.1:c.510G>T NP_001012745.1:p.Val170=
NM_006412.3:c.606G>T NP_006403.2:p.Val202=
NM_006412.4:c.606G>T MANE Select NP_006403.2:p.Val202=
NM_001012727.2:c.510G>T NP_001012745.1:p.Val170=