Canonical Allele Identifier: CA2742405536
Gene: SPSB1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.9348737C>A , CM000663.2:g.9348737C>A GRCh38
NC_000001.10:g.9408796C>A , CM000663.1:g.9408796C>A GRCh37
NC_000001.9:g.9331383C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000328089.11:c.-149-7006C>A MANE Select ENSP00000330221.6:n.-149-7006C>A
ENST00000328089.10:c.-149-7006C>A ENSP00000330221.6:n.-149-7006C>A
ENST00000450402.1:c.-149-7006C>A ENSP00000409235.1:n.-149-7006C>A
NM_025106.3:c.-149-7006C>A NP_079382.2:n.-149-7006C>A
NM_025106.4:c.-149-7006C>A MANE Select NP_079382.2:n.-149-7006C>A