Canonical Allele Identifier: CA207664086

Gene: PCDH15

Linked Data

• dbSNP Id: rs746487482
• gnomAD v2: 10-56790882-G-A
• gnomAD v3: 10-55031122-G-A
• gnomAD v4: 10-55031122-G-A
• MyVariant Identifiers: chr10:g.56790882G>A (hg19) ; chr10:g.55031122G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.55031122G>A , CM000672.2:g.55031122G>A	GRCh38
NC_000010.10:g.56790882G>A , CM000672.1:g.56790882G>A	GRCh37
NC_000010.9:g.56460888G>A	NCBI36
NG_009191.3:g.603061C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000458638.1:c.-79-133622C>T	ENSP00000394465.1:n.-79-133622C>T
ENST00000613346.4:c.-79-133622C>T	ENSP00000481211.1:n.-79-133622C>T
NM_001354404.1:c.-79-133622C>T	NP_001341333.1:n.-79-133622C>T
XM_017016573.2:c.-156-82521C>T	XP_016872062.1:n.-156-82521C>T
NM_001354404.2:c.-79-133622C>T	NP_001341333.1:n.-79-133622C>T