Canonical Allele Identifier: CA207648949
Gene: PCDH15 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs6481128

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.54901602G>A , CM000672.2:g.54901602G>A GRCh38
NC_000010.10:g.56661362G>A , CM000672.1:g.56661362G>A GRCh37
NC_000010.9:g.56331368G>A NCBI36
NG_009191.3:g.732581C>T

Transcript Alleles

HGVS Amino-acid change
NM_001354404.1:c.-79-4102C>T VV NP_001341333.1:p.=
XM_017016573.2:c.-79-4102C>T XP_016872062.1:p.=
ENST00000458638.1:c.-79-4102C>T ENSP00000394465.1:p.=
ENST00000613346.4:c.-79-4102C>T ENSP00000481211.1:p.=