Canonical Allele Identifier: CA721246459
Gene: PPL HGNC NCBI

Linked Data

dbSNP Id: rs1421441251
MyVariant Identifiers: chr16:g.5001231C>T (hg19) chr16:g.4951230C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.4951230C>T , CM000678.2:g.4951230C>T GRCh38
NC_000016.9:g.5001231C>T , CM000678.1:g.5001231C>T GRCh37
NC_000016.8:g.4941232C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000592772.1:c.-92+9334G>A ENSP00000467699.1:n.-92+9334G>A
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