Canonical Allele Identifier: CA277125626
Gene: PPL HGNC NCBI

Linked Data

dbSNP Id: rs989196443
MyVariant Identifiers: chr16:g.4951345T>C (hg38)

Genomic Alleles

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

Transcript Alleles

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