Canonical Allele Identifier: CA201623226

Gene: AGPAT2

Linked Data

• dbSNP Id: rs941656353
• MyVariant Identifiers: chr9:g.139568032G>A (hg19) ; chr9:g.136673580G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.136673580G>A , CM000671.2:g.136673580G>A	GRCh38
NC_000009.11:g.139568032G>A , CM000671.1:g.139568032G>A	GRCh37
NC_000009.10:g.138687853G>A	NCBI36
NG_008090.1:g.18880C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371696.7:c.*172C>T MANE Select	ENSP00000360761.2:n.*172C>T
ENST00000371694.7:c.*172C>T	ENSP00000360759.3:n.*172C>T
ENST00000371696.6:c.*172C>T	ENSP00000360761.2:n.*172C>T
ENST00000538402.1:c.*172C>T	ENSP00000438919.1:n.*172C>T
NM_001012727.1:c.*172C>T	NP_001012745.1:n.*172C>T
NM_006412.3:c.*172C>T	NP_006403.2:n.*172C>T
NM_006412.4:c.*172C>T MANE Select	NP_006403.2:n.*172C>T
NM_001012727.2:c.*172C>T	NP_001012745.1:n.*172C>T