Canonical Allele Identifier: CA519972371
Gene: PNPLA4P1 HGNC NCBI

Linked Data

MyVariant Identifiers: chrY:g.16192996A>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.14081116A>T , CM000686.2:g.14081116A>T GRCh38
NC_000024.9:g.16192996A>T , CM000686.1:g.16192996A>T GRCh37
NC_000024.8:g.14702390A>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000458328.1:n.42A>T
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