Canonical Allele Identifier: CA201641189

Gene: AGPAT2

Linked Data

• dbSNP Id: rs900767022
• gnomAD v3: 9-136687005-C-G
• gnomAD v4: 9-136687005-C-G
• MyVariant Identifiers: chr9:g.139581457C>G (hg19) ; chr9:g.136687005C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.136687005C>G , CM000671.2:g.136687005C>G	GRCh38
NC_000009.11:g.139581457C>G , CM000671.1:g.139581457C>G	GRCh37
NC_000009.10:g.138701278C>G	NCBI36
NG_008090.1:g.5455G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371696.7:c.182+171G>C MANE Select	ENSP00000360761.2:n.182+171G>C
ENST00000371694.7:c.182+171G>C	ENSP00000360759.3:n.182+171G>C
ENST00000371696.6:c.182+171G>C	ENSP00000360761.2:n.182+171G>C
ENST00000470861.1:n.190+171G>C
ENST00000538402.1:c.182+171G>C	ENSP00000438919.1:n.182+171G>C
NM_001012727.1:c.182+171G>C	NP_001012745.1:n.182+171G>C
NM_006412.3:c.182+171G>C	NP_006403.2:n.182+171G>C
NM_006412.4:c.182+171G>C MANE Select	NP_006403.2:n.182+171G>C
NM_001012727.2:c.182+171G>C	NP_001012745.1:n.182+171G>C