Canonical Allele Identifier: CA2203618813
Gene: PPL HGNC NCBI

Linked Data

dbSNP Id: rs2089422661

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.4951383T>C , CM000678.2:g.4951383T>C GRCh38
NC_000016.9:g.5001384T>C , CM000678.1:g.5001384T>C GRCh37
NC_000016.8:g.4941385T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000592772.1:c.-92+9181A>G ENSP00000467699.1:n.-92+9181A>G