Canonical Allele Identifier: CA721246561
Gene: PPL HGNC NCBI

Linked Data

dbSNP Id: rs989196443
gnomAD v3: 16-4951345-T-A
gnomAD v4: 16-4951345-T-A

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.4951345T>A , CM000678.2:g.4951345T>A GRCh38
NC_000016.9:g.5001346T>A , CM000678.1:g.5001346T>A GRCh37
NC_000016.8:g.4941347T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000592772.1:c.-92+9219A>T ENSP00000467699.1:n.-92+9219A>T