Canonical Allele Identifier: CA2203618591
Gene: PPL HGNC NCBI

Linked Data

dbSNP Id: rs2089421886

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.4951204G>C , CM000678.2:g.4951204G>C GRCh38
NC_000016.9:g.5001205G>C , CM000678.1:g.5001205G>C GRCh37
NC_000016.8:g.4941206G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000592772.1:c.-92+9360C>G ENSP00000467699.1:n.-92+9360C>G