Canonical Allele Identifier: CA1044886619
Gene: SSUH2 HGNC NCBI

Linked Data

dbSNP Id: rs780141299
gnomAD v3: 3-8733635-G-T
gnomAD v4: 3-8733635-G-T

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.8733635G>T , CM000665.2:g.8733635G>T GRCh38
NC_000003.11:g.8775321G>T , CM000665.1:g.8775321G>T GRCh37
NC_000003.10:g.8750321G>T NCBI36
NG_008797.2:g.4826G>T , LRG_329:g.4826G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000435138.5:c.64+8824C>A ENSP00000412333.1:n.64+8824C>A
ENST00000478513.1:n.335+8824C>A
XR_940435.1:n.330+8824C>A
XM_017006530.1:c.-283+8824C>A XP_016862019.1:n.-283+8824C>A