Canonical Allele Identifier: CA2620705874
Gene: WSCD2 HGNC NCBI

Linked Data

gnomAD v4: 12-108250445-C-A
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.108250445C>A , CM000674.2:g.108250445C>A GRCh38
NC_000012.11:g.108644222C>A , CM000674.1:g.108644222C>A GRCh37
NC_000012.10:g.107168352C>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000547525.6:c.*2102C>A MANE Select ENSP00000448047.1:n.*2102C>A
ENST00000332082.8:c.*2102C>A ENSP00000331933.4:n.*2102C>A
NM_001304447.1:c.*2102C>A NP_001291376.1:n.*2102C>A
NM_014653.3:c.*2102C>A NP_055468.2:n.*2102C>A
NM_014653.4:c.*2102C>A MANE Select NP_055468.2:n.*2102C>A
NM_001304447.2:c.*2102C>A NP_001291376.1:n.*2102C>A
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