Canonical Allele Identifier: CA1152754031
Gene: SPSB1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.9348833T= , CM000663.2:g.9348833T= GRCh38
NC_000001.10:g.9408892T= , CM000663.1:g.9408892T= GRCh37
NC_000001.9:g.9331479T= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000328089.11:c.-149-6910T= MANE Select ENSP00000330221.6:n.-149-6910T=
ENST00000328089.10:c.-149-6910T= ENSP00000330221.6:n.-149-6910T=
ENST00000450402.1:c.-149-6910T= ENSP00000409235.1:n.-149-6910T=
NM_025106.3:c.-149-6910T= NP_079382.2:n.-149-6910T=
NM_025106.4:c.-149-6910T= MANE Select NP_079382.2:n.-149-6910T=