Canonical Allele Identifier: CA951585806

Gene: WSCD2

Linked Data

• dbSNP Id: rs1890358425
• gnomAD v3: 12-108250228-A-G
• gnomAD v4: 12-108250228-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.108250228A>G , CM000674.2:g.108250228A>G	GRCh38
NC_000012.11:g.108644005A>G , CM000674.1:g.108644005A>G	GRCh37
NC_000012.10:g.107168135A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000547525.6:c.*1885A>G MANE Select	ENSP00000448047.1:n.*1885A>G
ENST00000332082.8:c.*1885A>G	ENSP00000331933.4:n.*1885A>G
NM_001304447.1:c.*1885A>G	NP_001291376.1:n.*1885A>G
NM_014653.3:c.*1885A>G	NP_055468.2:n.*1885A>G
NM_014653.4:c.*1885A>G MANE Select	NP_055468.2:n.*1885A>G
NM_001304447.2:c.*1885A>G	NP_001291376.1:n.*1885A>G