Canonical Allele Identifier: CA2692655498
Gene: AGPAT2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.136687430G>A , CM000671.2:g.136687430G>A GRCh38
NC_000009.11:g.139581882G>A , CM000671.1:g.139581882G>A GRCh37
NC_000009.10:g.138701703G>A NCBI36
NG_008090.1:g.5030C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000371696.7:c.-73C>T MANE Select ENSP00000360761.2:n.-73C>T
NM_001012727.1:c.-73C>T NP_001012745.1:n.-73C>T
NM_006412.3:c.-73C>T NP_006403.2:n.-73C>T
NM_006412.4:c.-73C>T MANE Select NP_006403.2:n.-73C>T
NM_001012727.2:c.-73C>T NP_001012745.1:n.-73C>T