Canonical Allele Identifier: CA1406373030
Gene: SPSB4 HGNC NCBI

Linked Data

dbSNP Id: rs16851055

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.141080371G>C , CM000665.2:g.141080371G>C GRCh38
NC_000003.11:g.140799213G>C , CM000665.1:g.140799213G>C GRCh37
NC_000003.10:g.142281903G>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000310546.3:c.694+13573G>C MANE Select ENSP00000311609.2:n.694+13573G>C
ENST00000310546.2:c.694+13573G>C ENSP00000311609.2:n.694+13573G>C
ENST00000507895.1:n.220G>C
ENST00000508126.1:c.161+13573G>C
ENST00000508828.1:n.535G>C
NM_080862.2:c.694+13573G>C NP_543138.1:n.694+13573G>C
XM_011513313.1:c.694+13573G>C XP_011511615.1:n.694+13573G>C
XR_924215.1:n.1510G>C
XR_924216.1:n.1510G>C
XM_017007509.2:c.*74G>C XP_016862998.1:n.*74G>C
XR_924215.3:n.991G>C
XR_924216.3:n.991G>C
NM_080862.3:c.694+13573G>C MANE Select NP_543138.1:n.694+13573G>C