Canonical Allele Identifier: CA620520654
Gene: PPL HGNC NCBI

Linked Data

dbSNP Id: rs1361940465
gnomAD v2: 16-5001417-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.4951416A>G , CM000678.2:g.4951416A>G GRCh38
NC_000016.9:g.5001417A>G , CM000678.1:g.5001417A>G GRCh37
NC_000016.8:g.4941418A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000592772.1:c.-92+9148T>C ENSP00000467699.1:n.-92+9148T>C