Canonical Allele Identifier: CA1344396255
Gene: SSUH2 HGNC NCBI

Linked Data

dbSNP Id: rs890355402
gnomAD v4: 3-8733775-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.8733775A>G , CM000665.2:g.8733775A>G GRCh38
NC_000003.11:g.8775461A>G , CM000665.1:g.8775461A>G GRCh37
NC_000003.10:g.8750461A>G NCBI36
NG_008797.2:g.4966A>G , LRG_329:g.4966A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000435138.5:c.64+8684T>C ENSP00000412333.1:n.64+8684T>C
ENST00000478513.1:n.335+8684T>C
XR_940435.1:n.330+8684T>C
XM_017006530.1:c.-283+8684T>C XP_016862019.1:n.-283+8684T>C