Canonical Allele Identifier: CA639583209
Gene: PNPLA3 HGNC NCBI

Linked Data

dbSNP Id: rs1225576857
gnomAD v2: 22-44324686-T-C
gnomAD v3: 22-43928806-T-C
gnomAD v4: 22-43928806-T-C
MyVariant Identifiers: chr22:g.44324686T>C (hg19) chr22:g.43928806T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.43928806T>C , CM000684.2:g.43928806T>C GRCh38
NC_000022.10:g.44324686T>C , CM000684.1:g.44324686T>C GRCh37
NC_000022.9:g.42656019T>C NCBI36
NG_008631.1:g.10068T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000216180.8:c.421-18T>C MANE Select ENSP00000216180.3:n.421-18T>C
ENST00000216180.7:c.421-18T>C ENSP00000216180.3:n.421-18T>C
ENST00000406117.6:c.*53-18T>C ENSP00000384668.2:n.*53-18T>C
ENST00000423180.2:c.409-18T>C ENSP00000397987.2:n.409-18T>C
ENST00000478713.1:n.455-18T>C
NM_025225.2:c.421-18T>C NP_079501.2:n.421-18T>C
NM_025225.3:c.421-18T>C MANE Select NP_079501.2:n.421-18T>C
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