Canonical Allele Identifier: CA2664269798
Gene: SSUH2 HGNC NCBI

Linked Data

gnomAD v4: 3-8733666-T-G

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.8733666T>G , CM000665.2:g.8733666T>G GRCh38
NC_000003.11:g.8775352T>G , CM000665.1:g.8775352T>G GRCh37
NC_000003.10:g.8750352T>G NCBI36
NG_008797.2:g.4857T>G , LRG_329:g.4857T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000435138.5:c.64+8793A>C ENSP00000412333.1:n.64+8793A>C
ENST00000478513.1:n.335+8793A>C
XR_940435.1:n.330+8793A>C
XM_017006530.1:c.-283+8793A>C XP_016862019.1:n.-283+8793A>C