Canonical Allele Identifier: CA1344396182
Gene: SSUH2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.8733718T= , CM000665.2:g.8733718T= GRCh38
NC_000003.11:g.8775404T= , CM000665.1:g.8775404T= GRCh37
NC_000003.10:g.8750404T= NCBI36
NG_008797.2:g.4909T= , LRG_329:g.4909T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000435138.5:c.64+8741A= ENSP00000412333.1:n.64+8741A=
ENST00000478513.1:n.335+8741A=
XR_940435.1:n.330+8741A=
XM_017006530.1:c.-283+8741A= XP_016862019.1:n.-283+8741A=