Canonical Allele Identifier: CA1152754071

Gene: SPSB1

Linked Data

• dbSNP Id: rs1640205283

Genomic Alleles

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

Transcript Alleles

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