Canonical Allele Identifier: CA889164501
Gene: SF3B4 HGNC NCBI

Linked Data

dbSNP Id: rs1464907292
MyVariant Identifiers: chr1:g.149927965T>A (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.149927965T>A , CM000663.2:g.149927965T>A GRCh38
NC_000001.10:g.149899857T>A , CM000663.1:g.149899857T>A GRCh37
NC_000001.9:g.148166481T>A NCBI36
NG_032777.1:g.5288A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000271628.8:c.-206A>T ENSP00000271628.8:n.-206A>T
NM_005850.4:c.-206A>T NP_005841.1:n.-206A>T