Canonical Allele Identifier: CA889164491
Gene: SF3B4 HGNC NCBI

Linked Data

dbSNP Id: rs1432180449
MyVariant Identifiers: chr1:g.149927961C>T (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.149927961C>T , CM000663.2:g.149927961C>T GRCh38
NC_000001.10:g.149899853C>T , CM000663.1:g.149899853C>T GRCh37
NC_000001.9:g.148166477C>T NCBI36
NG_032777.1:g.5292G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000271628.8:c.-202G>A ENSP00000271628.8:n.-202G>A
NM_005850.4:c.-202G>A NP_005841.1:n.-202G>A