Canonical Allele Identifier: CA2692653744
Gene: AGPAT2 HGNC NCBI

Linked Data

dbSNP Id: rs1846044000
gnomAD v4: 9-136673751-G-A
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.136673751G>A , CM000671.2:g.136673751G>A GRCh38
NC_000009.11:g.139568203G>A , CM000671.1:g.139568203G>A GRCh37
NC_000009.10:g.138688024G>A NCBI36
NG_008090.1:g.18709C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000371696.7:c.*1C>T MANE Select ENSP00000360761.2:n.*1C>T
ENST00000371694.7:c.*1C>T ENSP00000360759.3:n.*1C>T
ENST00000371696.6:c.*1C>T ENSP00000360761.2:n.*1C>T
ENST00000472820.1:n.766C>T
ENST00000538402.1:c.*1C>T ENSP00000438919.1:n.*1C>T
NM_001012727.1:c.*1C>T NP_001012745.1:n.*1C>T
NM_006412.3:c.*1C>T NP_006403.2:n.*1C>T
NM_006412.4:c.*1C>T MANE Select NP_006403.2:n.*1C>T
NM_001012727.2:c.*1C>T NP_001012745.1:n.*1C>T
Search 100 bp 5'
Search 100 bp 3'