Canonical Allele Identifier: CA201627695

Gene: AGPAT2

Linked Data

• dbSNP Id: rs17855341
• gnomAD v4: 9-136674798-C-A
• MyVariant Identifiers: chr9:g.139569250C>A (hg19) ; chr9:g.136674798C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.136674798C>A , CM000671.2:g.136674798C>A	GRCh38
NC_000009.11:g.139569250C>A , CM000671.1:g.139569250C>A	GRCh37
NC_000009.10:g.138689071C>A	NCBI36
NG_008090.1:g.17662G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371696.7:c.598G>T MANE Select	ENSP00000360761.2:p.Val200Phe
ENST00000371694.7:c.502G>T	ENSP00000360759.3:p.Val168Phe
ENST00000371696.6:c.598G>T	ENSP00000360761.2:p.Val200Phe
ENST00000472820.1:n.526G>T
ENST00000538402.1:c.598G>T	ENSP00000438919.1:p.Val200Phe
NM_001012727.1:c.502G>T	NP_001012745.1:p.Val168Phe
NM_006412.3:c.598G>T	NP_006403.2:p.Val200Phe
NM_006412.4:c.598G>T MANE Select	NP_006403.2:p.Val200Phe
NM_001012727.2:c.502G>T	NP_001012745.1:p.Val168Phe