Canonical Allele Identifier: CA2805673318
Gene: PPL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.4951403A>G , CM000678.2:g.4951403A>G GRCh38
NC_000016.9:g.5001404A>G , CM000678.1:g.5001404A>G GRCh37
NC_000016.8:g.4941405A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000592772.1:c.-92+9161T>C ENSP00000467699.1:n.-92+9161T>C