Canonical Allele Identifier: CA386719989

Gene: SH2B3

Linked Data

• MyVariant Identifiers: chr12:g.111856476C>G (hg19) ; chr12:g.111418672C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.111418672C>G , CM000674.2:g.111418672C>G	GRCh38
NC_000012.11:g.111856476C>G , CM000674.1:g.111856476C>G	GRCh37
NC_000012.10:g.110340859C>G	NCBI36
NG_021216.1:g.17725C>G , LRG_621:g.17725C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000341259.7:c.527C>G MANE Select	ENSP00000345492.2:p.Pro176Arg
ENST00000341259.6:c.527C>G	ENSP00000345492.2:p.Pro176Arg
ENST00000550925.2:c.333C>G
NM_005475.2:c.527C>G , LRG_621t1:c.527C>G	NP_005466.1:p.Pro176Arg
XM_005253818.3:c.527C>G	XP_005253875.1:p.Pro176Arg
XM_005253819.3:c.527C>G	XP_005253876.1:p.Pro176Arg
XM_011537719.1:c.527C>G	XP_011536021.1:p.Pro176Arg
XM_011537720.1:c.527C>G	XP_011536022.1:p.Pro176Arg
XM_011537722.1:c.527C>G	XP_011536024.1:p.Pro176Arg
XM_005253818.4:c.527C>G	XP_005253875.1:p.Pro176Arg
XM_005253819.4:c.527C>G	XP_005253876.1:p.Pro176Arg
XM_011537719.2:c.527C>G	XP_011536021.1:p.Pro176Arg
XM_011537720.3:c.527C>G	XP_011536022.1:p.Pro176Arg
XM_024448790.1:c.527C>G	XP_024304558.1:p.Pro176Arg
XR_001748535.1:n.928C>G
XR_001748536.1:n.927C>G
XR_002957278.1:n.924C>G
NM_005475.3:c.527C>G MANE Select	NP_005466.1:p.Pro176Arg