Canonical Allele Identifier: CA1344395622
Gene: SSUH2 HGNC NCBI

Linked Data

dbSNP Id: rs1707630136
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.8733340G>A , CM000665.2:g.8733340G>A GRCh38
NC_000003.11:g.8775026G>A , CM000665.1:g.8775026G>A GRCh37
NC_000003.10:g.8750026G>A NCBI36
NG_008797.2:g.4531G>A , LRG_329:g.4531G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000435138.5:c.64+9119C>T ENSP00000412333.1:n.64+9119C>T
ENST00000478513.1:n.335+9119C>T
XR_940435.1:n.330+9119C>T
XM_017006530.1:c.-283+9119C>T XP_016862019.1:n.-283+9119C>T
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