Canonical Allele Identifier: CA1152754062
Gene: SPSB1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.9348862C= , CM000663.2:g.9348862C= GRCh38
NC_000001.10:g.9408921C= , CM000663.1:g.9408921C= GRCh37
NC_000001.9:g.9331508C= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000328089.11:c.-149-6881C= MANE Select ENSP00000330221.6:n.-149-6881C=
ENST00000328089.10:c.-149-6881C= ENSP00000330221.6:n.-149-6881C=
ENST00000450402.1:c.-149-6881C= ENSP00000409235.1:n.-149-6881C=
NM_025106.3:c.-149-6881C= NP_079382.2:n.-149-6881C=
NM_025106.4:c.-149-6881C= MANE Select NP_079382.2:n.-149-6881C=
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