Canonical Allele Identifier: CA899796000

Gene: SPSB4

Linked Data

• dbSNP Id: rs1232692781
• MyVariant Identifiers: chr3:g.140799062G>T (hg19) ; chr3:g.141080220G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.141080220G>T , CM000665.2:g.141080220G>T	GRCh38
NC_000003.11:g.140799062G>T , CM000665.1:g.140799062G>T	GRCh37
NC_000003.10:g.142281752G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000310546.3:c.694+13422G>T MANE Select	ENSP00000311609.2:n.694+13422G>T
ENST00000310546.2:c.694+13422G>T	ENSP00000311609.2:n.694+13422G>T
ENST00000507895.1:n.139-70G>T
ENST00000508126.1:c.161+13422G>T
ENST00000508828.1:n.454-70G>T
NM_080862.2:c.694+13422G>T	NP_543138.1:n.694+13422G>T
XM_011513313.1:c.694+13422G>T	XP_011511615.1:n.694+13422G>T
XR_924215.1:n.1429-70G>T
XR_924216.1:n.1429-70G>T
XM_017007509.2:c.695-70G>T	XP_016862998.1:n.695-70G>T
XR_924215.3:n.910-70G>T
XR_924216.3:n.910-70G>T
NM_080862.3:c.694+13422G>T MANE Select	NP_543138.1:n.694+13422G>T