Canonical Allele Identifier: CA2581246606
Gene: PPL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.4951379A>T , CM000678.2:g.4951379A>T GRCh38
NC_000016.9:g.5001380A>T , CM000678.1:g.5001380A>T GRCh37
NC_000016.8:g.4941381A>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000592772.1:c.-92+9185T>A ENSP00000467699.1:n.-92+9185T>A