Canonical Allele Identifier: CA591367905

Gene: AGPAT2

Linked Data

• dbSNP Id: rs1238981495
• gnomAD v2: 9-139581900-C-A
• gnomAD v3: 9-136687448-C-A
• gnomAD v4: 9-136687448-C-A
• MyVariant Identifiers: chr9:g.139581900C>A (hg19) ; chr9:g.136687448C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.136687448C>A , CM000671.2:g.136687448C>A	GRCh38
NC_000009.11:g.139581900C>A , CM000671.1:g.139581900C>A	GRCh37
NC_000009.10:g.138701721C>A	NCBI36
NG_008090.1:g.5012G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371696.7:c.-91G>T MANE Select	ENSP00000360761.2:n.-91G>T
NM_001012727.1:c.-91G>T	NP_001012745.1:n.-91G>T
NM_006412.3:c.-91G>T	NP_006403.2:n.-91G>T
NM_006412.4:c.-91G>T MANE Select	NP_006403.2:n.-91G>T
NM_001012727.2:c.-91G>T	NP_001012745.1:n.-91G>T