Canonical Allele Identifier: CA917606306
Gene: SH3TC2 HGNC NCBI

Linked Data

dbSNP Id: rs869249332
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.148994658_148994660dup , CM000667.2:g.148994658_148994660dup GRCh38
NC_000005.9:g.148374221_148374223dup , CM000667.1:g.148374221_148374223dup GRCh37
NC_000005.8:g.148354414_148354416dup NCBI36
NG_007947.2:g.73516_73518dup , LRG_269:g.73516_73518dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000515425.6:c.*10052_*10054dup MANE Select ENSP00000423660.1:n.*10052_*10054dup
ENST00000504690.5:c.*12+9067_*12+9069dup ENSP00000425627.1:n.*12+9067_*12+9069dup
ENST00000510350.1:n.231+12222_231+12224dup
NM_024577.3:c.*10052_*10054dup , LRG_269t1:c.*10052_*10054dup NP_078853.2:n.*10052_*10054dup
NM_024577.4:c.*10052_*10054dup MANE Select NP_078853.2:n.*10052_*10054dup
Search 100 bp 5'
Search 100 bp 3'