Canonical Allele Identifier: CA519972298
Gene: PNPLA4P1 HGNC NCBI

Linked Data

MyVariant Identifiers: chrY:g.16192972C>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.14081092C>G , CM000686.2:g.14081092C>G GRCh38
NC_000024.9:g.16192972C>G , CM000686.1:g.16192972C>G GRCh37
NC_000024.8:g.14702366C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000458328.1:n.18C>G