Canonical Allele Identifier: CA889164582
Gene: SF3B4 HGNC NCBI

Linked Data

dbSNP Id: rs1236795895
MyVariant Identifiers: chr1:g.149928084A>T (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.149928084A>T , CM000663.2:g.149928084A>T GRCh38
NC_000001.10:g.149899976A>T , CM000663.1:g.149899976A>T GRCh37
NC_000001.9:g.148166600A>T NCBI36
NG_032777.1:g.5169T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000271628.8:c.-325T>A ENSP00000271628.8:n.-325T>A
NM_005850.4:c.-325T>A NP_005841.1:n.-325T>A