Canonical Allele Identifier: CA472352567

Gene: PNPLA2

Linked Data

• dbSNP Id: rs1845683608
• MyVariant Identifiers: chr11:g.822023G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.822023G>A , CM000673.2:g.822023G>A	GRCh38
NC_000011.9:g.822023G>A , CM000673.1:g.822023G>A	GRCh37
NC_000011.8:g.812023G>A	NCBI36
NG_023394.1:g.8123G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336615.9:c.486G>A MANE Select	ENSP00000337701.4:p.Val162=
ENST00000336615.8:c.486G>A	ENSP00000337701.4:p.Val162=
ENST00000525250.5:n.1092G>A
ENST00000531923.1:n.8G>A
ENST00000534561.1:n.153G>A
ENST00000617551.1:c.-765G>A	ENSP00000481602.1:n.-765G>A
NM_020376.3:c.486G>A	NP_065109.1:p.Val162=
XM_006718265.2:c.486G>A	XP_006718328.1:p.Val162=
XM_006718266.2:c.486G>A	XP_006718329.1:p.Val162=
XM_006718265.3:c.486G>A	XP_006718328.1:p.Val162=
XM_006718266.3:c.486G>A	XP_006718329.1:p.Val162=
XM_017018028.1:c.486G>A	XP_016873517.1:p.Val162=
XM_024448618.1:c.486G>A	XP_024304386.1:p.Val162=
NM_020376.4:c.486G>A MANE Select	NP_065109.1:p.Val162=