Canonical Allele Identifier: CA514856657
Gene: PNPLA3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr22:g.44324748C>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.43928868C>A , CM000684.2:g.43928868C>A GRCh38
NC_000022.10:g.44324748C>A , CM000684.1:g.44324748C>A GRCh37
NC_000022.9:g.42656081C>A NCBI36
NG_008631.1:g.10130C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000216180.8:c.465C>A MANE Select ENSP00000216180.3:p.Ile155=
ENST00000216180.7:c.465C>A ENSP00000216180.3:p.Ile155=
ENST00000406117.6:c.*97C>A ENSP00000384668.2:n.*97C>A
ENST00000423180.2:c.453C>A ENSP00000397987.2:p.Ile151=
ENST00000478713.1:n.499C>A
NM_025225.2:c.465C>A NP_079501.2:p.Ile155=
NM_025225.3:c.465C>A MANE Select NP_079501.2:p.Ile155=