Canonical Allele Identifier: CA2061868410
Gene: WSCD2 HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.108250223C= , CM000674.2:g.108250223C= GRCh38
NC_000012.11:g.108644000C= , CM000674.1:g.108644000C= GRCh37
NC_000012.10:g.107168130C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000547525.6:c.*1880C= MANE Select ENSP00000448047.1:n.*1880C=
ENST00000332082.8:c.*1880C= ENSP00000331933.4:n.*1880C=
NM_001304447.1:c.*1880C= NP_001291376.1:n.*1880C=
NM_014653.3:c.*1880C= NP_055468.2:n.*1880C=
NM_014653.4:c.*1880C= MANE Select NP_055468.2:n.*1880C=
NM_001304447.2:c.*1880C= NP_001291376.1:n.*1880C=
Search 100 bp 5'
Search 100 bp 3'