Canonical Allele Identifier: CA916830557
Gene: SSUH2 HGNC NCBI

Linked Data

dbSNP Id: rs1559639119

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.8733564_8733573dup , CM000665.2:g.8733564_8733573dup GRCh38
NC_000003.11:g.8775250_8775259dup , CM000665.1:g.8775250_8775259dup GRCh37
NC_000003.10:g.8750250_8750259dup NCBI36
NG_008797.2:g.4755_4764dup , LRG_329:g.4755_4764dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000435138.5:c.64+8886_64+8895dup ENSP00000412333.1:n.64+8886_64+8895dup
ENST00000478513.1:n.335+8886_335+8895dup
XR_940435.1:n.330+8886_330+8895dup
XM_017006530.1:c.-283+8886_-283+8895dup XP_016862019.1:n.-283+8886_-283+8895dup