Canonical Allele Identifier: CA2805673314
Gene: PPL HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.4951211C>A , CM000678.2:g.4951211C>A GRCh38
NC_000016.9:g.5001212C>A , CM000678.1:g.5001212C>A GRCh37
NC_000016.8:g.4941213C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000592772.1:c.-92+9353G>T ENSP00000467699.1:n.-92+9353G>T
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