Canonical Allele Identifier: CA1344395660
Gene: SSUH2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.8733377A= , CM000665.2:g.8733377A= GRCh38
NC_000003.11:g.8775063A= , CM000665.1:g.8775063A= GRCh37
NC_000003.10:g.8750063A= NCBI36
NG_008797.2:g.4568A= , LRG_329:g.4568A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000435138.5:c.64+9082T= ENSP00000412333.1:n.64+9082T=
ENST00000478513.1:n.335+9082T=
XR_940435.1:n.330+9082T=
XM_017006530.1:c.-283+9082T= XP_016862019.1:n.-283+9082T=