Canonical Allele Identifier: CA2203618748
Gene: PPL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.4951344A= , CM000678.2:g.4951344A= GRCh38
NC_000016.9:g.5001345A= , CM000678.1:g.5001345A= GRCh37
NC_000016.8:g.4941346A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000592772.1:c.-92+9220T= ENSP00000467699.1:n.-92+9220T=