Canonical Allele Identifier: CA69861776
Gene: SSUH2 HGNC NCBI

Linked Data

dbSNP Id: rs990749912
gnomAD v3: 3-8733722-T-C
gnomAD v4: 3-8733722-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.8733722T>C , CM000665.2:g.8733722T>C GRCh38
NC_000003.11:g.8775408T>C , CM000665.1:g.8775408T>C GRCh37
NC_000003.10:g.8750408T>C NCBI36
NG_008797.2:g.4913T>C , LRG_329:g.4913T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000435138.5:c.64+8737A>G ENSP00000412333.1:n.64+8737A>G
ENST00000478513.1:n.335+8737A>G
XR_940435.1:n.330+8737A>G
XM_017006530.1:c.-283+8737A>G XP_016862019.1:n.-283+8737A>G