Canonical Allele Identifier: CA386720527
Gene: SH2B3 HGNC NCBI
Revel Score:
gnomAD v4:

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.111418767G>A , CM000674.2:g.111418767G>A GRCh38
NC_000012.11:g.111856571G>A , CM000674.1:g.111856571G>A GRCh37
NC_000012.10:g.110340954G>A NCBI36
NG_021216.1:g.17820G>A , LRG_621:g.17820G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000341259.7:c.622G>A MANE Select ENSP00000345492.2:p.Glu208Lys
ENST00000341259.6:c.622G>A ENSP00000345492.2:p.Glu208Lys
ENST00000550925.2:c.428G>A
NM_005475.2:c.622G>A , LRG_621t1:c.622G>A NP_005466.1:p.Glu208Lys
XM_005253818.3:c.622G>A XP_005253875.1:p.Glu208Lys
XM_005253819.3:c.622G>A XP_005253876.1:p.Glu208Lys
XM_011537719.1:c.622G>A XP_011536021.1:p.Glu208Lys
XM_011537720.1:c.622G>A XP_011536022.1:p.Glu208Lys
XM_011537722.1:c.622G>A XP_011536024.1:p.Glu208Lys
XM_005253818.4:c.622G>A XP_005253875.1:p.Glu208Lys
XM_005253819.4:c.622G>A XP_005253876.1:p.Glu208Lys
XM_011537719.2:c.622G>A XP_011536021.1:p.Glu208Lys
XM_011537720.3:c.622G>A XP_011536022.1:p.Glu208Lys
XM_024448790.1:c.622G>A XP_024304558.1:p.Glu208Lys
XR_001748535.1:n.1023G>A
XR_001748536.1:n.1022G>A
XR_002957278.1:n.1019G>A
NM_005475.3:c.622G>A MANE Select NP_005466.1:p.Glu208Lys