Canonical Allele Identifier: CA352915336

Gene: SEMA3B

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000616701.5:c.1244C>A MANE Select	ENSP00000484146.1:p.Thr415Asn
ENST00000418576.3:c.215C>A	ENSP00000485173.1:p.Thr72Asn
ENST00000419007.5:n.1040C>A
ENST00000433753.4:c.1241C>A	ENSP00000485281.1:p.Thr414Asn
ENST00000439487.5:n.533C>A
ENST00000441915.5:n.1240C>A
ENST00000456210.5:n.377C>A
ENST00000456560.6:c.215C>A	ENSP00000485646.1:p.Thr72Asn
ENST00000611067.4:c.1259C>A	ENSP00000480680.1:p.Thr420Asn
ENST00000611418.4:c.1243C>A	ENSP00000484583.1:p.Leu415Met
ENST00000616701.4:c.1244C>A	ENSP00000484146.1:p.Thr415Asn
ENST00000618865.4:c.1244C>A	ENSP00000481957.1:p.Thr415Asn
ENST00000619119.4:n.1719C>A
NM_001005914.2:c.1241C>A	NP_001005914.1:p.Thr414Asn
NM_001290060.1:c.1244C>A	NP_001276989.1:p.Thr415Asn
NM_001290061.1:c.1259C>A	NP_001276990.1:p.Thr420Asn
NM_001290062.1:c.215C>A	NP_001276991.1:p.Thr72Asn
NM_001290063.1:c.215C>A	NP_001276992.1:p.Thr72Asn
NM_004636.3:c.1244C>A	NP_004627.1:p.Thr415Asn
NR_110697.1:n.415C>A
NM_001290060.2:c.1244C>A MANE Select	NP_001276989.1:p.Thr415Asn
NM_001005914.3:c.1241C>A	NP_001005914.1:p.Thr414Asn
NM_001290062.2:c.215C>A	NP_001276991.1:p.Thr72Asn
NM_001290063.2:c.215C>A	NP_001276992.1:p.Thr72Asn
NM_004636.4:c.1244C>A	NP_004627.1:p.Thr415Asn