Canonical Allele Identifier: CA1152754070
Gene: SPSB1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.9348867C= , CM000663.2:g.9348867C= GRCh38
NC_000001.10:g.9408926C= , CM000663.1:g.9408926C= GRCh37
NC_000001.9:g.9331513C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000328089.11:c.-149-6876C= MANE Select ENSP00000330221.6:n.-149-6876C=
ENST00000328089.10:c.-149-6876C= ENSP00000330221.6:n.-149-6876C=
ENST00000450402.1:c.-149-6876C= ENSP00000409235.1:n.-149-6876C=
NM_025106.3:c.-149-6876C= NP_079382.2:n.-149-6876C=
NM_025106.4:c.-149-6876C= MANE Select NP_079382.2:n.-149-6876C=