Canonical Allele Identifier: CA861081149

Gene: AGPAT2

Linked Data

• dbSNP Id: rs1488240115
• gnomAD v3: 9-136674633-G-A
• gnomAD v4: 9-136674633-G-A
• MyVariant Identifiers: chr9:g.139569085G>A (hg19) ; chr9:g.136674633G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.136674633G>A , CM000671.2:g.136674633G>A	GRCh38
NC_000009.11:g.139569085G>A , CM000671.1:g.139569085G>A	GRCh37
NC_000009.10:g.138688906G>A	NCBI36
NG_008090.1:g.17827C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000371696.7:c.661+102C>T MANE Select	ENSP00000360761.2:n.661+102C>T
ENST00000371694.7:c.565+102C>T	ENSP00000360759.3:n.565+102C>T
ENST00000371696.6:c.661+102C>T	ENSP00000360761.2:n.661+102C>T
ENST00000472820.1:n.589+102C>T
ENST00000538402.1:c.661+102C>T	ENSP00000438919.1:n.661+102C>T
NM_001012727.1:c.565+102C>T	NP_001012745.1:n.565+102C>T
NM_006412.3:c.661+102C>T	NP_006403.2:n.661+102C>T
NM_006412.4:c.661+102C>T MANE Select	NP_006403.2:n.661+102C>T
NM_001012727.2:c.565+102C>T	NP_001012745.1:n.565+102C>T