Canonical Allele Identifier: CA1344395620
Gene: SSUH2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.8733338G= , CM000665.2:g.8733338G= GRCh38
NC_000003.11:g.8775024G= , CM000665.1:g.8775024G= GRCh37
NC_000003.10:g.8750024G= NCBI36
NG_008797.2:g.4529G= , LRG_329:g.4529G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000435138.5:c.64+9121C= ENSP00000412333.1:n.64+9121C=
ENST00000478513.1:n.335+9121C=
XR_940435.1:n.330+9121C=
XM_017006530.1:c.-283+9121C= XP_016862019.1:n.-283+9121C=