Canonical Allele Identifier: CA161771186
Gene: SEMA3A HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs10235789

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.84027484T>C , CM000669.2:g.84027484T>C GRCh38
NC_000007.13:g.83656800T>C , CM000669.1:g.83656800T>C GRCh37
NC_000007.12:g.83494736T>C NCBI36
NG_011489.1:g.172418A>G

Transcript Alleles

HGVS Amino-acid change
NM_006080.2:c.668-13133A>G VV NP_006071.1:p.=
XM_005250110.2:c.668-13133A>G XP_005250167.1:p.=
XM_005250111.3:c.668-13133A>G XP_005250168.1:p.=
XM_006715839.2:c.668-13133A>G XP_006715902.1:p.=
XM_011515734.1:c.668-13133A>G XP_011514036.1:p.=
XM_011515735.1:c.668-13133A>G XP_011514037.1:p.=
XM_005250110.3:c.668-13133A>G XP_005250167.1:p.=
XM_005250111.4:c.668-13133A>G XP_005250168.1:p.=
XM_006715839.3:c.668-13133A>G XP_006715902.1:p.=
XM_011515734.3:c.668-13133A>G XP_011514036.1:p.=
XM_017011673.1:c.668-13133A>G XP_016867162.1:p.=
XM_024446633.1:c.668-13133A>G XP_024302401.1:p.=
NM_006080.3:c.668-13133A>G VV MANE Preferred NP_006071.1:p.=
ENST00000265362.8:c.668-13133A>G ENSP00000265362.3:p.=
ENST00000436949.5:c.668-13133A>G ENSP00000415260.1:p.=