Canonical Allele Identifier: CA2731788176
Gene: PPL HGNC NCBI

Linked Data

dbSNP Id: rs2142455076

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.4951423G>T , CM000678.2:g.4951423G>T GRCh38
NC_000016.9:g.5001424G>T , CM000678.1:g.5001424G>T GRCh37
NC_000016.8:g.4941425G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000592772.1:c.-92+9141C>A ENSP00000467699.1:n.-92+9141C>A