Canonical Allele Identifier: CA324876792
Gene: PNPLA3 HGNC NCBI

Linked Data

dbSNP Id: rs925810242
gnomAD v2: 22-44325028-A-C
gnomAD v3: 22-43929148-A-C
gnomAD v4: 22-43929148-A-C
MyVariant Identifiers: chr22:g.44325028A>C (hg19) chr22:g.43929148A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.43929148A>C , CM000684.2:g.43929148A>C GRCh38
NC_000022.10:g.44325028A>C , CM000684.1:g.44325028A>C GRCh37
NC_000022.9:g.42656361A>C NCBI36
NG_008631.1:g.10410A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000216180.8:c.486+259A>C MANE Select ENSP00000216180.3:n.486+259A>C
ENST00000216180.7:c.486+259A>C ENSP00000216180.3:n.486+259A>C
ENST00000406117.6:c.*118+259A>C ENSP00000384668.2:n.*118+259A>C
ENST00000423180.2:c.474+259A>C ENSP00000397987.2:n.474+259A>C
ENST00000478713.1:n.520+259A>C
NM_025225.2:c.486+259A>C NP_079501.2:n.486+259A>C
NM_025225.3:c.486+259A>C MANE Select NP_079501.2:n.486+259A>C
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