Canonical Allele Identifier: CA721246640
Gene: PPL HGNC NCBI

Linked Data

dbSNP Id: rs1327423211
gnomAD v3: 16-4951437-A-G
gnomAD v4: 16-4951437-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.4951437A>G , CM000678.2:g.4951437A>G GRCh38
NC_000016.9:g.5001438A>G , CM000678.1:g.5001438A>G GRCh37
NC_000016.8:g.4941439A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000592772.1:c.-92+9127T>C ENSP00000467699.1:n.-92+9127T>C