Canonical Allele Identifier: CA1344396233
Gene: SSUH2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.8733755C= , CM000665.2:g.8733755C= GRCh38
NC_000003.11:g.8775441C= , CM000665.1:g.8775441C= GRCh37
NC_000003.10:g.8750441C= NCBI36
NG_008797.2:g.4946C= , LRG_329:g.4946C=

Transcript Alleles

HGVS Amino-acid change
ENST00000435138.5:c.64+8704G= ENSP00000412333.1:n.64+8704G=
ENST00000478513.1:n.335+8704G=
XR_940435.1:n.330+8704G=
XM_017006530.1:c.-283+8704G= XP_016862019.1:n.-283+8704G=