Canonical Allele Identifier: CA13321041
Gene: PCDH15 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs16906916

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.55089225A>C , CM000672.2:g.55089225A>C GRCh38
NC_000010.10:g.56848985A>C , CM000672.1:g.56848985A>C GRCh37
NC_000010.9:g.56518991A>C NCBI36
NG_009191.3:g.544958T>G

Transcript Alleles

HGVS Amino-acid change
NM_001354404.1:c.-80+77351T>G VV NP_001341333.1:p.=
XM_017016573.2:c.-157+77351T>G XP_016872062.1:p.=
ENST00000458638.1:c.-80+77351T>G ENSP00000394465.1:p.=
ENST00000613346.4:c.-80+77351T>G ENSP00000481211.1:p.=