Canonical Allele Identifier: CA2664269898
Gene: SSUH2 HGNC NCBI

Linked Data

gnomAD v4: 3-8733754-G-A
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.8733754G>A , CM000665.2:g.8733754G>A GRCh38
NC_000003.11:g.8775440G>A , CM000665.1:g.8775440G>A GRCh37
NC_000003.10:g.8750440G>A NCBI36
NG_008797.2:g.4945G>A , LRG_329:g.4945G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000435138.5:c.64+8705C>T ENSP00000412333.1:n.64+8705C>T
ENST00000478513.1:n.335+8705C>T
XR_940435.1:n.330+8705C>T
XM_017006530.1:c.-283+8705C>T XP_016862019.1:n.-283+8705C>T
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