Canonical Allele Identifier: CA889164025
Gene: SF3B4 HGNC NCBI

Linked Data

dbSNP Id: rs1158591170
MyVariant Identifiers: chr1:g.149927809del (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.149927809del , CM000663.2:g.149927809del GRCh38
NC_000001.10:g.149899701del , CM000663.1:g.149899701del GRCh37
NC_000001.9:g.148166325del NCBI36
NG_032777.1:g.5444del

Transcript Alleles

HGVS Amino-acid Change
ENST00000271628.8:c.-50del ENSP00000271628.8:n.-50del
NM_005850.4:c.-50del NP_005841.1:n.-50del