Canonical Allele Identifier: CA1044886413
Gene: SSUH2 HGNC NCBI

Linked Data

dbSNP Id: rs1707631888
gnomAD v3: 3-8733424-A-G
gnomAD v4: 3-8733424-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.8733424A>G , CM000665.2:g.8733424A>G GRCh38
NC_000003.11:g.8775110A>G , CM000665.1:g.8775110A>G GRCh37
NC_000003.10:g.8750110A>G NCBI36
NG_008797.2:g.4615A>G , LRG_329:g.4615A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000435138.5:c.64+9035T>C ENSP00000412333.1:n.64+9035T>C
ENST00000478513.1:n.335+9035T>C
XR_940435.1:n.330+9035T>C
XM_017006530.1:c.-283+9035T>C XP_016862019.1:n.-283+9035T>C