Canonical Allele Identifier: CA889164050
Gene: SF3B4 HGNC NCBI

Linked Data

dbSNP Id: rs1330772386
MyVariant Identifiers: chr1:g.149927839G>T (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.149927839G>T , CM000663.2:g.149927839G>T GRCh38
NC_000001.10:g.149899731G>T , CM000663.1:g.149899731G>T GRCh37
NC_000001.9:g.148166355G>T NCBI36
NG_032777.1:g.5414C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000271628.8:c.-80C>A ENSP00000271628.8:n.-80C>A
NM_005850.4:c.-80C>A NP_005841.1:n.-80C>A