Canonical Allele Identifier: CA11130602
Gene: RBMS1 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs6718526

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.160357664T>C , CM000664.2:g.160357664T>C GRCh38
NC_000002.11:g.161214175T>C , CM000664.1:g.161214175T>C GRCh37
NC_000002.10:g.160922421T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
NM_002897.4:c.251+9552A>G VV NP_002888.1:p.=
NM_016836.3:c.251+9552A>G VV NP_058520.1:p.=
XM_005246737.1:c.251+9552A>G XP_005246794.1:p.=
XM_005246738.2:c.248+9552A>G XP_005246795.1:p.=
XM_005246739.2:c.245+9552A>G XP_005246796.1:p.=
XM_005246740.1:c.251+9552A>G XP_005246797.1:p.=
XM_005246741.3:c.242+9552A>G XP_005246798.1:p.=
XM_006712671.2:c.257+9552A>G XP_006712734.1:p.=
XM_006712672.2:c.257+9552A>G XP_006712735.1:p.=
XM_006712673.2:c.257+9552A>G XP_006712736.1:p.=
XM_006712674.2:c.257+9552A>G XP_006712737.1:p.=
XM_005246738.3:c.248+9552A>G XP_005246795.1:p.=
XM_017004626.2:c.248+9552A>G XP_016860115.1:p.=
XM_024453032.1:c.248+9552A>G XP_024308800.1:p.=
XM_024453033.1:c.245+9552A>G XP_024308801.1:p.=
XM_024453034.1:c.245+9552A>G XP_024308802.1:p.=
NM_016836.4:c.251+9552A>G VV MANE Preferred NP_058520.1:p.=
ENST00000348849.7:c.251+9552A>G ENSP00000294904.6:p.=
ENST00000392753.7:n.191+9552A>G ENSP00000376508.4:p.=
ENST00000409075.5:c.152+9552A>G ENSP00000386347.1:p.=
ENST00000409289.6:c.152+9552A>G ENSP00000386571.2:p.=
ENST00000409972.5:c.152+9552A>G ENSP00000387280.1:p.=
ENST00000428519.1:c.152+9552A>G ENSP00000389016.1:p.=
ENST00000474820.5:n.377+9552A>G
ENST00000491781.5:n.370+9552A>G