Canonical Allele Identifier: CA514856652
Gene: PNPLA3 HGNC NCBI

Linked Data

dbSNP Id: rs2049942748
MyVariant Identifiers: chr22:g.44324742C>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.43928862C>G , CM000684.2:g.43928862C>G GRCh38
NC_000022.10:g.44324742C>G , CM000684.1:g.44324742C>G GRCh37
NC_000022.9:g.42656075C>G NCBI36
NG_008631.1:g.10124C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000216180.8:c.459C>G MANE Select ENSP00000216180.3:p.Gly153=
ENST00000216180.7:c.459C>G ENSP00000216180.3:p.Gly153=
ENST00000406117.6:c.*91C>G ENSP00000384668.2:n.*91C>G
ENST00000423180.2:c.447C>G ENSP00000397987.2:p.Gly149=
ENST00000478713.1:n.493C>G
NM_025225.2:c.459C>G NP_079501.2:p.Gly153=
NM_025225.3:c.459C>G MANE Select NP_079501.2:p.Gly153=
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