Canonical Allele Identifier: CA2692653786
Gene: AGPAT2 HGNC NCBI

Linked Data

gnomAD v4: 9-136673940-C-A
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.136673940C>A , CM000671.2:g.136673940C>A GRCh38
NC_000009.11:g.139568392C>A , CM000671.1:g.139568392C>A GRCh37
NC_000009.10:g.138688213C>A NCBI36
NG_008090.1:g.18520G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000371696.7:c.662-13G>T MANE Select ENSP00000360761.2:n.662-13G>T
ENST00000371694.7:c.566-13G>T ENSP00000360759.3:n.566-13G>T
ENST00000371696.6:c.662-13G>T ENSP00000360761.2:n.662-13G>T
ENST00000472820.1:n.590-13G>T
ENST00000538402.1:c.662-13G>T ENSP00000438919.1:n.662-13G>T
NM_001012727.1:c.566-13G>T NP_001012745.1:n.566-13G>T
NM_006412.3:c.662-13G>T NP_006403.2:n.662-13G>T
NM_006412.4:c.662-13G>T MANE Select NP_006403.2:n.662-13G>T
NM_001012727.2:c.566-13G>T NP_001012745.1:n.566-13G>T
Search 100 bp 5'
Search 100 bp 3'