Canonical Allele Identifier: CA1344396252

Gene: SSUH2

Linked Data

• dbSNP Id: rs2072583

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.8733771G>C , CM000665.2:g.8733771G>C	GRCh38
NC_000003.11:g.8775457G>C , CM000665.1:g.8775457G>C	GRCh37
NC_000003.10:g.8750457G>C	NCBI36
NG_008797.2:g.4962G>C , LRG_329:g.4962G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000435138.5:c.64+8688C>G	ENSP00000412333.1:n.64+8688C>G
ENST00000478513.1:n.335+8688C>G
XR_940435.1:n.330+8688C>G
XM_017006530.1:c.-283+8688C>G	XP_016862019.1:n.-283+8688C>G