Canonical Allele Identifier: CA889164461
Gene: SF3B4 HGNC NCBI

Linked Data

dbSNP Id: rs1018531739
MyVariant Identifiers: chr1:g.149927949C>T (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.149927949C>T , CM000663.2:g.149927949C>T GRCh38
NC_000001.10:g.149899841C>T , CM000663.1:g.149899841C>T GRCh37
NC_000001.9:g.148166465C>T NCBI36
NG_032777.1:g.5304G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000271628.8:c.-190G>A ENSP00000271628.8:n.-190G>A
NM_005850.4:c.-190G>A NP_005841.1:n.-190G>A