Canonical Allele Identifier: CA1152754028
Gene: SPSB1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.9348825A= , CM000663.2:g.9348825A= GRCh38
NC_000001.10:g.9408884A= , CM000663.1:g.9408884A= GRCh37
NC_000001.9:g.9331471A= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000328089.11:c.-149-6918A= MANE Select ENSP00000330221.6:n.-149-6918A=
ENST00000328089.10:c.-149-6918A= ENSP00000330221.6:n.-149-6918A=
ENST00000450402.1:c.-149-6918A= ENSP00000409235.1:n.-149-6918A=
NM_025106.3:c.-149-6918A= NP_079382.2:n.-149-6918A=
NM_025106.4:c.-149-6918A= MANE Select NP_079382.2:n.-149-6918A=