Canonical Allele Identifier: CA639583304
Gene: PNPLA3 HGNC NCBI

Linked Data

dbSNP Id: rs1224323676
gnomAD v2: 22-44325033-T-C
gnomAD v3: 22-43929153-T-C
gnomAD v4: 22-43929153-T-C
MyVariant Identifiers: chr22:g.44325033T>C (hg19) chr22:g.43929153T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.43929153T>C , CM000684.2:g.43929153T>C GRCh38
NC_000022.10:g.44325033T>C , CM000684.1:g.44325033T>C GRCh37
NC_000022.9:g.42656366T>C NCBI36
NG_008631.1:g.10415T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000216180.8:c.486+264T>C MANE Select ENSP00000216180.3:n.486+264T>C
ENST00000216180.7:c.486+264T>C ENSP00000216180.3:n.486+264T>C
ENST00000406117.6:c.*118+264T>C ENSP00000384668.2:n.*118+264T>C
ENST00000423180.2:c.474+264T>C ENSP00000397987.2:n.474+264T>C
ENST00000478713.1:n.520+264T>C
NM_025225.2:c.486+264T>C NP_079501.2:n.486+264T>C
NM_025225.3:c.486+264T>C MANE Select NP_079501.2:n.486+264T>C
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