Canonical Allele Identifier: CA1142339891
Gene: SF3B4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.149926178T= , CM000663.2:g.149926178T= GRCh38
NC_000001.10:g.149898070T= , CM000663.1:g.149898070T= GRCh37
NC_000001.9:g.148164694T= NCBI36
NG_032777.1:g.7075A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000271628.9:c.707-136A= MANE Select ENSP00000271628.8:n.707-136A=
ENST00000271628.8:c.707-136A= ENSP00000271628.8:n.707-136A=
NM_005850.4:c.707-136A= NP_005841.1:n.707-136A=
NM_005850.5:c.707-136A= MANE Select NP_005841.1:n.707-136A=