Canonical Allele Identifier: CA1620615209
Gene: SNRPC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.34762706A= , CM000668.2:g.34762706A= GRCh38
NC_000006.11:g.34730483A= , CM000668.1:g.34730483A= GRCh37
NC_000006.10:g.34838461A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000244520.10:c.160+3A= MANE Select ENSP00000244520.5:n.160+3A=
ENST00000244520.9:c.160+3A= ENSP00000244520.5:n.160+3A=
ENST00000374017.3:c.223+3A= ENSP00000363129.3:n.223+3A=
ENST00000374018.5:c.37+3A= ENSP00000363130.1:n.37+3A=
ENST00000474635.1:n.152+3A=
NM_003093.2:c.160+3A= NP_003084.1:n.160+3A=
NR_029472.1:n.567+3A=
NM_003093.3:c.160+3A= MANE Select NP_003084.1:n.160+3A=
NR_029472.2:n.156+3A=