Canonical Allele Identifier: CA1363873237

Gene: SEMA3B

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.50274469C= , CM000665.2:g.50274469C=	GRCh38
NC_000003.11:g.50311900C= , CM000665.1:g.50311900C=	GRCh37
NC_000003.10:g.50286904C=	NCBI36
NG_032938.1:g.11862C=

Transcript Alleles

HGVS	Amino-acid Change
NM_001290060.2:c.1244C= MANE Select	NP_001276989.1:p.Thr415=
ENST00000616701.5:c.1244C= MANE Select	ENSP00000484146.1:p.Thr415=
NM_001005914.2:c.1241C=	NP_001005914.1:p.Thr414=
NM_001005914.3:c.1241C=	NP_001005914.1:p.Thr414=
NM_001290060.1:c.1244C=	NP_001276989.1:p.Thr415=
NM_001290061.1:c.1259C=	NP_001276990.1:p.Thr420=
NM_001290062.1:c.215C=	NP_001276991.1:p.Thr72=
NM_001290062.2:c.215C=	NP_001276991.1:p.Thr72=
NM_001290063.1:c.215C=	NP_001276992.1:p.Thr72=
NM_001290063.2:c.215C=	NP_001276992.1:p.Thr72=
NM_004636.3:c.1244C=	NP_004627.1:p.Thr415=
NM_004636.4:c.1244C=	NP_004627.1:p.Thr415=
NR_110697.1:n.415C=
ENST00000418576.3:c.215C=	ENSP00000485173.1:p.Thr72=
ENST00000419007.5:n.1040C=
ENST00000433753.4:c.1241C=	ENSP00000485281.1:p.Thr414=
ENST00000439487.5:n.533C=
ENST00000441915.5:n.1240C=
ENST00000456210.5:n.377C=
ENST00000456560.6:c.215C=	ENSP00000485646.1:p.Thr72=
ENST00000611067.4:c.1259C=	ENSP00000480680.1:p.Thr420=
ENST00000611418.4:c.1243C=	ENSP00000484583.1:p.Leu415=
ENST00000616701.4:c.1244C=	ENSP00000484146.1:p.Thr415=
ENST00000618865.4:c.1244C=	ENSP00000481957.1:p.Thr415=
ENST00000619119.4:n.1719C=