Canonical Allele Identifier: CA74603741
Gene: SEMA3F HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs2072054

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.50159190A>G , CM000665.2:g.50159190A>G GRCh38
NC_000003.11:g.50196623A>G , CM000665.1:g.50196623A>G GRCh37
NC_000003.10:g.50171627A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
NM_004186.3:c.-48-385A>G VV NP_004177.3:p.=
XM_005265381.3:c.-48-385A>G XP_005265438.1:p.=
XM_005265382.3:c.-48-385A>G XP_005265439.1:p.=
XM_006713290.2:c.-48-385A>G XP_006713353.1:p.=
XM_011533998.1:c.-48-385A>G XP_011532300.1:p.=
XM_011533999.1:c.-147A>G XP_011532301.1:p.=
XM_011534000.1:c.-48-385A>G XP_011532302.1:p.=
XR_940487.1:n.150-385A>G
NM_001318798.1:c.-135-502A>G VV NP_001305727.1:p.=
NM_001318800.1:c.-147A>G VV NP_001305729.1:p.=
NM_004186.4:c.-48-385A>G VV
XM_005265381.4:c.-48-385A>G
XM_005265382.4:c.-48-385A>G
XM_006713290.3:c.-48-385A>G
XM_011533998.2:c.-48-385A>G
XM_011534000.2:c.-48-385A>G
XR_940487.2:n.88-385A>G
NM_004186.5:c.-48-385A>G VV MANE Preferred
ENST00000002829.7:c.-48-385A>G ENSP00000002829.3:p.=
ENST00000413852.5:c.-135-502A>G ENSP00000388931.1:p.=
ENST00000414301.5:c.-40-393A>G ENSP00000392588.1:p.=
ENST00000426511.5:c.-48-385A>G ENSP00000400549.1:p.=
ENST00000434342.5:c.-147A>G ENSP00000409859.1:p.=
ENST00000450338.5:c.-48-385A>G ENSP00000398399.1:p.=