Canonical Allele Identifier: CA2203618882
Gene: PPL HGNC NCBI

Linked Data

dbSNP Id: rs561390783
gnomAD v3: 16-4951436-A-T
gnomAD v4: 16-4951436-A-T

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.4951436A>T , CM000678.2:g.4951436A>T GRCh38
NC_000016.9:g.5001437A>T , CM000678.1:g.5001437A>T GRCh37
NC_000016.8:g.4941438A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000592772.1:c.-92+9128T>A ENSP00000467699.1:n.-92+9128T>A