Canonical Allele Identifier: CA1344395613

Gene: SSUH2

Linked Data

• dbSNP Id: rs1707629836

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.8733330C>T , CM000665.2:g.8733330C>T	GRCh38
NC_000003.11:g.8775016C>T , CM000665.1:g.8775016C>T	GRCh37
NC_000003.10:g.8750016C>T	NCBI36
NG_008797.2:g.4521C>T , LRG_329:g.4521C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000435138.5:c.64+9129G>A	ENSP00000412333.1:n.64+9129G>A
ENST00000478513.1:n.335+9129G>A
XR_940435.1:n.330+9129G>A
XM_017006530.1:c.-283+9129G>A	XP_016862019.1:n.-283+9129G>A