Canonical Allele Identifier: CA74587958

Gene: SEMA3F

Linked Data

• dbSNP Id: rs192672815
• gnomAD v2: 3-50211993-G-A
• gnomAD v3: 3-50174560-G-A
• gnomAD v4: 3-50174560-G-A
• MyVariant Identifiers: chr3:g.50211993G>A (hg19) ; chr3:g.50174560G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.50174560G>A , CM000665.2:g.50174560G>A	GRCh38
NC_000003.11:g.50211993G>A , CM000665.1:g.50211993G>A	GRCh37
NC_000003.10:g.50186997G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000002829.8:c.456+210G>A MANE Select	ENSP00000002829.3:n.456+210G>A
ENST00000002829.7:c.456+210G>A	ENSP00000002829.3:n.456+210G>A
ENST00000413852.5:c.252+210G>A	ENSP00000388931.1:n.252+210G>A
ENST00000414301.5:c.456+210G>A	ENSP00000392588.1:n.456+210G>A
ENST00000420831.1:c.348+210G>A	ENSP00000416356.1:n.348+210G>A
ENST00000434342.5:c.456+210G>A	ENSP00000409859.1:n.456+210G>A
ENST00000450338.5:c.456+210G>A	ENSP00000398399.1:n.456+210G>A
NM_004186.3:c.456+210G>A	NP_004177.3:n.456+210G>A
XM_005265381.3:c.456+210G>A	XP_005265438.1:n.456+210G>A
XM_005265382.3:c.456+210G>A	XP_005265439.1:n.456+210G>A
XM_006713290.2:c.456+210G>A	XP_006713353.1:n.456+210G>A
XM_011533998.1:c.456+210G>A	XP_011532300.1:n.456+210G>A
XM_011533999.1:c.456+210G>A	XP_011532301.1:n.456+210G>A
XM_011534000.1:c.456+210G>A	XP_011532302.1:n.456+210G>A
XR_940487.1:n.653+210G>A
NM_001318798.1:c.252+210G>A	NP_001305727.1:n.252+210G>A
NM_001318800.1:c.456+210G>A	NP_001305729.1:n.456+210G>A
NM_004186.4:c.456+210G>A	NP_004177.3:n.456+210G>A
XM_005265381.4:c.456+210G>A	XP_005265438.1:n.456+210G>A
XM_005265382.4:c.456+210G>A	XP_005265439.1:n.456+210G>A
XM_006713290.3:c.456+210G>A	XP_006713353.1:n.456+210G>A
XM_011533998.2:c.456+210G>A	XP_011532300.1:n.456+210G>A
XM_011534000.2:c.456+210G>A	XP_011532302.1:n.456+210G>A
XR_940487.2:n.591+210G>A
NM_004186.5:c.456+210G>A MANE Select	NP_004177.3:n.456+210G>A
NM_001318798.2:c.252+210G>A	NP_001305727.1:n.252+210G>A
NM_001318800.2:c.456+210G>A	NP_001305729.1:n.456+210G>A