Canonical Allele Identifier: CA11470040
Gene: RBMS3 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs10510628

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.29811912G>A , CM000665.2:g.29811912G>A GRCh38
NC_000003.11:g.29853403G>A , CM000665.1:g.29853403G>A GRCh37
NC_000003.10:g.29828407G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
NM_001003792.2:c.634+48923G>A VV NP_001003792.1:p.=
NM_001003793.2:c.637+48923G>A VV NP_001003793.1:p.=
NM_001177711.1:c.637+48923G>A VV NP_001171182.1:p.=
NM_001177712.1:c.637+48923G>A VV NP_001171183.1:p.=
NM_014483.3:c.637+48923G>A VV NP_055298.2:p.=
XM_005265060.1:c.634+48923G>A XP_005265117.1:p.=
XM_005265061.1:c.637+48923G>A XP_005265118.1:p.=
XM_005265062.1:c.637+48923G>A XP_005265119.1:p.=
XM_005265063.1:c.352+48923G>A XP_005265120.1:p.=
XM_005265064.3:c.352+48923G>A XP_005265121.1:p.=
XM_005265065.3:c.310+48923G>A XP_005265122.1:p.=
XM_011533592.1:c.637+48923G>A XP_011531894.1:p.=
XM_011533593.1:c.637+48923G>A XP_011531895.1:p.=
XM_011533594.1:c.637+48923G>A XP_011531896.1:p.=
NM_001330696.1:c.634+48923G>A VV NP_001317625.1:p.=
XM_005265061.2:c.637+48923G>A
XM_005265063.2:c.352+48923G>A
XM_005265065.5:c.310+48923G>A
XM_017006178.1:c.634+48923G>A XP_016861667.1:p.=
XM_017006179.1:c.634+48923G>A XP_016861668.1:p.=
XM_017006180.1:c.637+48923G>A XP_016861669.1:p.=
XM_017006181.1:c.634+48923G>A XP_016861670.1:p.=
XM_017006182.1:c.535+48923G>A XP_016861671.1:p.=
XM_024453454.1:c.637+48923G>A XP_024309222.1:p.=
ENST00000273139.13:c.637+48923G>A ENSP00000273139.9:p.=
ENST00000383766.6:c.634+48923G>A ENSP00000373276.2:p.=
ENST00000383767.6:c.637+48923G>A ENSP00000373277.2:p.=
ENST00000434693.6:c.634+48923G>A ENSP00000395592.1:p.=
ENST00000445033.5:c.637+48923G>A ENSP00000391934.1:p.=
ENST00000452462.5:c.637+48923G>A ENSP00000397926.1:p.=
ENST00000456853.1:c.637+48923G>A ENSP00000400519.1:p.=
ENST00000497319.1:n.67+48923G>A