Canonical Allele Identifier: CA1344395617
Gene: SSUH2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.8733333G= , CM000665.2:g.8733333G= GRCh38
NC_000003.11:g.8775019G= , CM000665.1:g.8775019G= GRCh37
NC_000003.10:g.8750019G= NCBI36
NG_008797.2:g.4524G= , LRG_329:g.4524G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000435138.5:c.64+9126C= ENSP00000412333.1:n.64+9126C=
ENST00000478513.1:n.335+9126C=
XR_940435.1:n.330+9126C=
XM_017006530.1:c.-283+9126C= XP_016862019.1:n.-283+9126C=