Canonical Allele Identifier: CA2063284244

Gene: SH2B3

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.111418673T= , CM000674.2:g.111418673T=	GRCh38
NC_000012.11:g.111856477T= , CM000674.1:g.111856477T=	GRCh37
NC_000012.10:g.110340860T=	NCBI36
NG_021216.1:g.17726T= , LRG_621:g.17726T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000341259.7:c.528T= MANE Select	ENSP00000345492.2:p.Pro176=
ENST00000341259.6:c.528T=	ENSP00000345492.2:p.Pro176=
ENST00000550925.2:c.334T=
NM_005475.2:c.528T= , LRG_621t1:c.528T=	NP_005466.1:p.Pro176=
XM_005253818.3:c.528T=	XP_005253875.1:p.Pro176=
XM_005253819.3:c.528T=	XP_005253876.1:p.Pro176=
XM_011537719.1:c.528T=	XP_011536021.1:p.Pro176=
XM_011537720.1:c.528T=	XP_011536022.1:p.Pro176=
XM_011537722.1:c.528T=	XP_011536024.1:p.Pro176=
XM_005253818.4:c.528T=	XP_005253875.1:p.Pro176=
XM_005253819.4:c.528T=	XP_005253876.1:p.Pro176=
XM_011537719.2:c.528T=	XP_011536021.1:p.Pro176=
XM_011537720.3:c.528T=	XP_011536022.1:p.Pro176=
XM_024448790.1:c.528T=	XP_024304558.1:p.Pro176=
XR_001748535.1:n.929T=
XR_001748536.1:n.928T=
XR_002957278.1:n.925T=
NM_005475.3:c.528T= MANE Select	NP_005466.1:p.Pro176=