Canonical Allele Identifier: CA974016041
Gene: PPL HGNC NCBI

Linked Data

gnomAD v3: 16-4951347-T-A
gnomAD v4: 16-4951347-T-A

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.4951347T>A , CM000678.2:g.4951347T>A GRCh38
NC_000016.9:g.5001348T>A , CM000678.1:g.5001348T>A GRCh37
NC_000016.8:g.4941349T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000592772.1:c.-92+9217A>T ENSP00000467699.1:n.-92+9217A>T