Canonical Allele Identifier: CA519972383
Gene: PNPLA4P1 HGNC NCBI

Linked Data

MyVariant Identifiers: chrY:g.16193000C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.14081120C>T , CM000686.2:g.14081120C>T GRCh38
NC_000024.9:g.16193000C>T , CM000686.1:g.16193000C>T GRCh37
NC_000024.8:g.14702394C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000458328.1:n.46C>T