Canonical Allele Identifier: CA519972338
Gene: PNPLA4P1 HGNC NCBI

Linked Data

MyVariant Identifiers: chrY:g.16192985G>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.14081105G>T , CM000686.2:g.14081105G>T GRCh38
NC_000024.9:g.16192985G>T , CM000686.1:g.16192985G>T GRCh37
NC_000024.8:g.14702379G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000458328.1:n.31G>T
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