Canonical Allele Identifier: CA515082889
Gene: PNPLA3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr22:g.44342181C>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.43946301C>T , CM000684.2:g.43946301C>T GRCh38
NC_000022.10:g.44342181C>T , CM000684.1:g.44342181C>T GRCh37
NC_000022.9:g.42673514C>T NCBI36
NG_008631.1:g.27563C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000216180.8:c.1365C>T MANE Select ENSP00000216180.3:p.Asn455=
ENST00000216180.7:c.1365C>T ENSP00000216180.3:p.Asn455=
ENST00000406117.6:c.*849+1506C>T ENSP00000384668.2:n.*849+1506C>T
ENST00000423180.2:c.1353C>T ENSP00000397987.2:p.Asn451=
NM_025225.2:c.1365C>T NP_079501.2:p.Asn455=
NM_025225.3:c.1365C>T MANE Select NP_079501.2:p.Asn455=
Search 100 bp 5'
Search 100 bp 3'