Canonical Allele Identifier: CA1344396001
Gene: SSUH2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.8733584C= , CM000665.2:g.8733584C= GRCh38
NC_000003.11:g.8775270C= , CM000665.1:g.8775270C= GRCh37
NC_000003.10:g.8750270C= NCBI36
NG_008797.2:g.4775C= , LRG_329:g.4775C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000435138.5:c.64+8875G= ENSP00000412333.1:n.64+8875G=
ENST00000478513.1:n.335+8875G=
XR_940435.1:n.330+8875G=
XM_017006530.1:c.-283+8875G= XP_016862019.1:n.-283+8875G=