Canonical Allele Identifier: CA277125630
Gene: PPL HGNC NCBI

Linked Data

dbSNP Id: rs915070478

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.4951349C>A , CM000678.2:g.4951349C>A GRCh38
NC_000016.9:g.5001350C>A , CM000678.1:g.5001350C>A GRCh37
NC_000016.8:g.4941351C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000592772.1:c.-92+9215G>T ENSP00000467699.1:n.-92+9215G>T