Canonical Allele Identifier: CA1344396224
Gene: SSUH2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.8733750T= , CM000665.2:g.8733750T= GRCh38
NC_000003.11:g.8775436T= , CM000665.1:g.8775436T= GRCh37
NC_000003.10:g.8750436T= NCBI36
NG_008797.2:g.4941T= , LRG_329:g.4941T=

Transcript Alleles

HGVS Amino-acid change
ENST00000435138.5:c.64+8709A= ENSP00000412333.1:n.64+8709A=
ENST00000478513.1:n.335+8709A=
XR_940435.1:n.330+8709A=
XM_017006530.1:c.-283+8709A= XP_016862019.1:n.-283+8709A=