Canonical Allele Identifier: CA1620615151
Gene: SNRPC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.34762519A= , CM000668.2:g.34762519A= GRCh38
NC_000006.11:g.34730296A= , CM000668.1:g.34730296A= GRCh37
NC_000006.10:g.34838274A= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000244520.10:c.52-76A= MANE Select ENSP00000244520.5:n.52-76A=
ENST00000244520.9:c.52-76A= ENSP00000244520.5:n.52-76A=
ENST00000374017.3:c.115-76A= ENSP00000363129.3:n.115-76A=
ENST00000374018.5:c.-72-76A= ENSP00000363130.1:n.-72-76A=
ENST00000474635.1:n.44-76A=
NM_003093.2:c.52-76A= NP_003084.1:n.52-76A=
NR_029472.1:n.459-76A=
NM_003093.3:c.52-76A= MANE Select NP_003084.1:n.52-76A=
NR_029472.2:n.48-76A=