Canonical Allele Identifier: CA2581246607
Gene: PPL HGNC NCBI

Genomic Alleles

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

Transcript Alleles

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