Canonical Allele Identifier: CA2664269878
Gene: SSUH2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.8733744_8733745insTTGG , CM000665.2:g.8733744_8733745insTTGG GRCh38
NC_000003.11:g.8775430_8775431insTTGG , CM000665.1:g.8775430_8775431insTTGG GRCh37
NC_000003.10:g.8750430_8750431insTTGG NCBI36
NG_008797.2:g.4935_4936insTTGG , LRG_329:g.4935_4936insTTGG

Transcript Alleles

HGVS Amino-acid change
ENST00000435138.5:c.64+8715_64+8716insCAAC ENSP00000412333.1:n.64+8715_64+8716insCAA...
ENST00000478513.1:n.335+8715_335+8716insCAAC
XR_940435.1:n.330+8715_330+8716insCAAC
XM_017006530.1:c.-283+8715_-283+8716insCAAC XP_016862019.1:n.-283+8715_-283+8716insCA...