Canonical Allele Identifier: CA2588730894
Gene: PCDH15 HGNC NCBI

Linked Data

dbSNP Id: rs2131825876

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.54901622A>T , CM000672.2:g.54901622A>T GRCh38
NC_000010.10:g.56661382A>T , CM000672.1:g.56661382A>T GRCh37
NC_000010.9:g.56331388A>T NCBI36
NG_009191.3:g.732561T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000458638.1:c.-79-4122T>A ENSP00000394465.1:n.-79-4122T>A
ENST00000613346.4:c.-79-4122T>A ENSP00000481211.1:n.-79-4122T>A
NM_001354404.1:c.-79-4122T>A NP_001341333.1:n.-79-4122T>A
XM_017016573.2:c.-79-4122T>A XP_016872062.1:n.-79-4122T>A
NM_001354404.2:c.-79-4122T>A NP_001341333.1:n.-79-4122T>A