Canonical Allele Identifier: CA889161586

Gene: SF3B4

Linked Data

• dbSNP Id: rs1401626269
• MyVariant Identifiers: chr1:g.149926090_149926091del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.149926090_149926091del , CM000663.2:g.149926090_149926091del	GRCh38
NC_000001.10:g.149897982_149897983del , CM000663.1:g.149897982_149897983del	GRCh37
NC_000001.9:g.148164606_148164607del	NCBI36
NG_032777.1:g.7162_7163del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000271628.9:c.707-49_707-48del MANE Select	ENSP00000271628.8:n.707-49_707-48del
ENST00000271628.8:c.707-49_707-48del	ENSP00000271628.8:n.707-49_707-48del
NM_005850.4:c.707-49_707-48del	NP_005841.1:n.707-49_707-48del
NM_005850.5:c.707-49_707-48del MANE Select	NP_005841.1:n.707-49_707-48del