Canonical Allele Identifier: CA69861668
Gene: SSUH2 HGNC NCBI

Linked Data

dbSNP Id: rs200956747
gnomAD v2: 3-8775222-C-T
gnomAD v3: 3-8733536-C-T
gnomAD v4: 3-8733536-C-T
MyVariant Identifiers: chr3:g.8775222C>T (hg19) chr3:g.8733536C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.8733536C>T , CM000665.2:g.8733536C>T GRCh38
NC_000003.11:g.8775222C>T , CM000665.1:g.8775222C>T GRCh37
NC_000003.10:g.8750222C>T NCBI36
NG_008797.2:g.4727C>T , LRG_329:g.4727C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000435138.5:c.64+8923G>A ENSP00000412333.1:n.64+8923G>A
ENST00000478513.1:n.335+8923G>A
XR_940435.1:n.330+8923G>A
XM_017006530.1:c.-283+8923G>A XP_016862019.1:n.-283+8923G>A
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