Canonical Allele Identifier: CA2478942655
Gene: SF3B4 HGNC NCBI

Linked Data

dbSNP Id: rs2092598399

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.149927534C>T , CM000663.2:g.149927534C>T GRCh38
NC_000001.10:g.149899426C>T , CM000663.1:g.149899426C>T GRCh37
NC_000001.9:g.148166050C>T NCBI36
NG_032777.1:g.5719G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000271628.9:c.34+192G>A MANE Select ENSP00000271628.8:n.34+192G>A
ENST00000271628.8:c.34+192G>A ENSP00000271628.8:n.34+192G>A
ENST00000457312.1:c.-198G>A ENSP00000391114.1:n.-198G>A
NM_005850.4:c.34+192G>A NP_005841.1:n.34+192G>A
NM_005850.5:c.34+192G>A MANE Select NP_005841.1:n.34+192G>A