Canonical Allele Identifier: CA10277922
Gene: PNPLA3 HGNC NCBI

Linked Data

dbSNP Id: rs139051

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.43928796A>G , CM000684.2:g.43928796A>G GRCh38
NC_000022.10:g.44324676A>G , CM000684.1:g.44324676A>G GRCh37
NC_000022.9:g.42656009A>G NCBI36
NG_008631.1:g.10058A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000216180.8:c.421-28A>G MANE Select ENSP00000216180.3:n.421-28A>G
ENST00000216180.7:c.421-28A>G ENSP00000216180.3:n.421-28A>G
ENST00000406117.6:c.*53-28A>G ENSP00000384668.2:n.*53-28A>G
ENST00000423180.2:c.409-28A>G ENSP00000397987.2:n.409-28A>G
ENST00000478713.1:n.455-28A>G
NM_025225.2:c.421-28A>G NP_079501.2:n.421-28A>G
NM_025225.3:c.421-28A>G MANE Select NP_079501.2:n.421-28A>G