Canonical Allele Identifier: CA29992410
Gene: SF3B4 HGNC NCBI

Linked Data

dbSNP Id: rs946014915
MyVariant Identifiers: chr1:g.149928044C>A (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.149928044C>A , CM000663.2:g.149928044C>A GRCh38
NC_000001.10:g.149899936C>A , CM000663.1:g.149899936C>A GRCh37
NC_000001.9:g.148166560C>A NCBI36
NG_032777.1:g.5209G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000271628.8:c.-285G>T ENSP00000271628.8:n.-285G>T
NM_005850.4:c.-285G>T NP_005841.1:n.-285G>T