Canonical Allele Identifier: CA10651441
Gene: PNPLA3 HGNC NCBI

Linked Data

ClinVar Variation Id: 341949
ClinVar RCV Id: RCV000292212
dbSNP Id: rs2294919
gnomAD v2: 22-44342325-C-T
gnomAD v3: 22-43946445-C-T
gnomAD v4: 22-43946445-C-T
MyVariant Identifiers: chr22:g.44342325C>T (hg19) chr22:g.43946445C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.43946445C>T , CM000684.2:g.43946445C>T GRCh38
NC_000022.10:g.44342325C>T , CM000684.1:g.44342325C>T GRCh37
NC_000022.9:g.42673658C>T NCBI36
NG_008631.1:g.27707C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000216180.8:c.*63C>T MANE Select ENSP00000216180.3:n.*63C>T
ENST00000216180.7:c.*63C>T ENSP00000216180.3:n.*63C>T
ENST00000406117.6:c.*849+1650C>T ENSP00000384668.2:n.*849+1650C>T
ENST00000423180.2:c.*63C>T ENSP00000397987.2:n.*63C>T
NM_025225.2:c.*63C>T NP_079501.2:n.*63C>T
NM_025225.3:c.*63C>T MANE Select NP_079501.2:n.*63C>T
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