Canonical Allele Identifier: CA1406373006

Gene: SPSB4

Linked Data

• dbSNP Id: rs1938206153

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.141080312A>C , CM000665.2:g.141080312A>C	GRCh38
NC_000003.11:g.140799154A>C , CM000665.1:g.140799154A>C	GRCh37
NC_000003.10:g.142281844A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000310546.3:c.694+13514A>C MANE Select	ENSP00000311609.2:n.694+13514A>C
ENST00000310546.2:c.694+13514A>C	ENSP00000311609.2:n.694+13514A>C
ENST00000507895.1:n.161A>C
ENST00000508126.1:c.161+13514A>C
ENST00000508828.1:n.476A>C
NM_080862.2:c.694+13514A>C	NP_543138.1:n.694+13514A>C
XM_011513313.1:c.694+13514A>C	XP_011511615.1:n.694+13514A>C
XR_924215.1:n.1451A>C
XR_924216.1:n.1451A>C
XM_017007509.2:c.*15A>C	XP_016862998.1:n.*15A>C
XR_924215.3:n.932A>C
XR_924216.3:n.932A>C
NM_080862.3:c.694+13514A>C MANE Select	NP_543138.1:n.694+13514A>C