Canonical Allele Identifier: CA10608058
Gene: SF3B4 HGNC NCBI

Linked Data

ClinVar Variation Id: 292490
ClinVar RCV Id: RCV000302978
dbSNP Id: rs762430957

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.149928022dup , CM000663.2:g.149928022dup GRCh38
NC_000001.10:g.149899914dup , CM000663.1:g.149899914dup GRCh37
NC_000001.9:g.148166538dup NCBI36
NG_032777.1:g.5231dup

Transcript Alleles

HGVS Amino-acid change
ENST00000271628.8:c.-263dup ENSP00000271628.8:n.-263dup
NM_005850.4:c.-263dup NP_005841.1:n.-263dup