Canonical Allele Identifier: CA201623201
Gene: AGPAT2 HGNC NCBI

Linked Data

dbSNP Id: rs55754159

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.136673544G>A , CM000671.2:g.136673544G>A GRCh38
NC_000009.11:g.139567996G>A , CM000671.1:g.139567996G>A GRCh37
NC_000009.10:g.138687817G>A NCBI36
NG_008090.1:g.18916C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000371696.7:c.*208C>T MANE Select ENSP00000360761.2:n.*208C>T
ENST00000371694.7:c.*208C>T ENSP00000360759.3:n.*208C>T
ENST00000371696.6:c.*208C>T ENSP00000360761.2:n.*208C>T
ENST00000538402.1:c.*208C>T ENSP00000438919.1:n.*208C>T
NM_001012727.1:c.*208C>T NP_001012745.1:n.*208C>T
NM_006412.3:c.*208C>T NP_006403.2:n.*208C>T
NM_006412.4:c.*208C>T MANE Select NP_006403.2:n.*208C>T
NM_001012727.2:c.*208C>T NP_001012745.1:n.*208C>T