Canonical Allele Identifier: CA277125722
Gene: PPL HGNC NCBI

Linked Data

dbSNP Id: rs938965196
gnomAD v2: 16-5001430-C-T
gnomAD v3: 16-4951429-C-T
gnomAD v4: 16-4951429-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.4951429C>T , CM000678.2:g.4951429C>T GRCh38
NC_000016.9:g.5001430C>T , CM000678.1:g.5001430C>T GRCh37
NC_000016.8:g.4941431C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000592772.1:c.-92+9135G>A ENSP00000467699.1:n.-92+9135G>A