Canonical Allele Identifier: CA2664269931
Gene: SSUH2 HGNC NCBI

Linked Data

gnomAD v4: 3-8733780-T-A
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.8733780T>A , CM000665.2:g.8733780T>A GRCh38
NC_000003.11:g.8775466T>A , CM000665.1:g.8775466T>A GRCh37
NC_000003.10:g.8750466T>A NCBI36
NG_008797.2:g.4971T>A , LRG_329:g.4971T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000435138.5:c.64+8679A>T ENSP00000412333.1:n.64+8679A>T
ENST00000478513.1:n.335+8679A>T
XR_940435.1:n.330+8679A>T
XM_017006530.1:c.-283+8679A>T XP_016862019.1:n.-283+8679A>T
Search 100 bp 5'
Search 100 bp 3'