Canonical Allele Identifier: CA2203618632
Gene: PPL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.4951237T= , CM000678.2:g.4951237T= GRCh38
NC_000016.9:g.5001238T= , CM000678.1:g.5001238T= GRCh37
NC_000016.8:g.4941239T= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000592772.1:c.-92+9327A= ENSP00000467699.1:n.-92+9327A=