Canonical Allele Identifier: CA1620615195
Gene: SNRPC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.34762627G= , CM000668.2:g.34762627G= GRCh38
NC_000006.11:g.34730404G= , CM000668.1:g.34730404G= GRCh37
NC_000006.10:g.34838382G= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000244520.10:c.84G= MANE Select ENSP00000244520.5:p.Arg28=
ENST00000244520.9:c.84G= ENSP00000244520.5:p.Arg28=
ENST00000374017.3:c.147G= ENSP00000363129.3:p.Arg49=
ENST00000374018.5:c.-40G= ENSP00000363130.1:n.-40G=
ENST00000474635.1:n.76G=
NM_003093.2:c.84G= NP_003084.1:p.Arg28=
NR_029472.1:n.491G=
NM_003093.3:c.84G= MANE Select NP_003084.1:p.Arg28=
NR_029472.2:n.80G=