Canonical Allele Identifier: CA2664269822

Gene: SSUH2

Linked Data

• gnomAD v4: 3-8733688-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.8733688A>G , CM000665.2:g.8733688A>G	GRCh38
NC_000003.11:g.8775374A>G , CM000665.1:g.8775374A>G	GRCh37
NC_000003.10:g.8750374A>G	NCBI36
NG_008797.2:g.4879A>G , LRG_329:g.4879A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000435138.5:c.64+8771T>C	ENSP00000412333.1:n.64+8771T>C
ENST00000478513.1:n.335+8771T>C
XR_940435.1:n.330+8771T>C
XM_017006530.1:c.-283+8771T>C	XP_016862019.1:n.-283+8771T>C