Canonical Allele Identifier: CA2620933464
Gene: SH2B3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.111418675del , CM000674.2:g.111418675del GRCh38
NC_000012.11:g.111856479del , CM000674.1:g.111856479del GRCh37
NC_000012.10:g.110340862del NCBI36
NG_021216.1:g.17728del , LRG_621:g.17728del

Transcript Alleles

HGVS Amino-acid Change
ENST00000341259.7:c.530del MANE Select ENSP00000345492.2:p.Gly177AlafsTer20
ENST00000341259.6:c.530del ENSP00000345492.2:p.Gly177AlafsTer20
ENST00000550925.2:c.336del
NM_005475.2:c.530del , LRG_621t1:c.530del NP_005466.1:p.Gly177AlafsTer20
XM_005253818.3:c.530del XP_005253875.1:p.Gly177AlafsTer20
XM_005253819.3:c.530del XP_005253876.1:p.Gly177AlafsTer20
XM_011537719.1:c.530del XP_011536021.1:p.Gly177AlafsTer20
XM_011537720.1:c.530del XP_011536022.1:p.Gly177AlafsTer20
XM_011537722.1:c.530del XP_011536024.1:p.Gly177AlafsTer20
XM_005253818.4:c.530del XP_005253875.1:p.Gly177AlafsTer20
XM_005253819.4:c.530del XP_005253876.1:p.Gly177AlafsTer20
XM_011537719.2:c.530del XP_011536021.1:p.Gly177AlafsTer20
XM_011537720.3:c.530del XP_011536022.1:p.Gly177AlafsTer20
XM_024448790.1:c.530del XP_024304558.1:p.Gly177AlafsTer20
XR_001748535.1:n.931del
XR_001748536.1:n.930del
XR_002957278.1:n.927del
NM_005475.3:c.530del MANE Select NP_005466.1:p.Gly177AlafsTer20