Canonical Allele Identifier: CA14114893
Gene: SNRPN HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs2047433

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.24883191T>G , CM000677.2:g.24883191T>G GRCh38
NC_000015.9:g.25128338T>G , CM000677.1:g.25128338T>G GRCh37
NC_000015.8:g.22679431T>G NCBI36
NG_012958.1:g.64545T>G

Transcript Alleles

HGVS Amino-acid change
NM_022805.2:c.-578-3325T>G VV NP_073716.1:p.=
NM_022806.2:c.-578-3325T>G VV NP_073717.1:p.=
NM_022807.2:c.-578-3325T>G VV NP_073718.1:p.=
NM_022808.2:c.-578-3325T>G VV NP_073719.1:p.=
NM_001349454.1:c.-801-3325T>G VV NP_001336383.1:p.=
NM_001349455.1:c.-746-3325T>G VV NP_001336384.1:p.=
NM_001349456.1:c.-653-3325T>G VV NP_001336385.1:p.=
NM_001349457.1:c.-746-3325T>G VV NP_001336386.1:p.=
NM_001349458.1:c.-578-3325T>G VV NP_001336387.1:p.=
NM_001349459.1:c.-504-36820T>G VV NP_001336388.1:p.=
NM_001349460.1:c.-821-3325T>G VV NP_001336389.1:p.=
NM_001349461.1:c.-653-3325T>G VV NP_001336390.1:p.=
NM_001349462.1:c.-746-3325T>G VV NP_001336391.1:p.=
NM_022805.4:c.-578-3325T>G VV
NM_022806.4:c.-578-3325T>G VV
NM_022807.4:c.-578-3325T>G VV
NM_022808.4:c.-578-3325T>G VV
NR_146177.1:n.325-3325T>G
ENST00000400097.5:c.-578-3325T>G ENSP00000382969.1:p.=
ENST00000400098.6:n.188-3325T>G
ENST00000400100.5:c.-578-3325T>G ENSP00000382972.1:p.=
ENST00000553597.5:n.117-3325T>G