Canonical Allele Identifier: CA2664269882
Gene: SSUH2 HGNC NCBI

Linked Data

gnomAD v4: 3-8733745-C-G

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.8733745C>G , CM000665.2:g.8733745C>G GRCh38
NC_000003.11:g.8775431C>G , CM000665.1:g.8775431C>G GRCh37
NC_000003.10:g.8750431C>G NCBI36
NG_008797.2:g.4936C>G , LRG_329:g.4936C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000435138.5:c.64+8714G>C ENSP00000412333.1:n.64+8714G>C
ENST00000478513.1:n.335+8714G>C
XR_940435.1:n.330+8714G>C
XM_017006530.1:c.-283+8714G>C XP_016862019.1:n.-283+8714G>C