Canonical Allele Identifier: CA1620615162
Gene: SNRPC HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.34762545T= , CM000668.2:g.34762545T= GRCh38
NC_000006.11:g.34730322T= , CM000668.1:g.34730322T= GRCh37
NC_000006.10:g.34838300T= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000244520.10:c.52-50T= MANE Select ENSP00000244520.5:n.52-50T=
ENST00000244520.9:c.52-50T= ENSP00000244520.5:n.52-50T=
ENST00000374017.3:c.115-50T= ENSP00000363129.3:n.115-50T=
ENST00000374018.5:c.-72-50T= ENSP00000363130.1:n.-72-50T=
ENST00000474635.1:n.44-50T=
NM_003093.2:c.52-50T= NP_003084.1:n.52-50T=
NR_029472.1:n.459-50T=
NM_003093.3:c.52-50T= MANE Select NP_003084.1:n.52-50T=
NR_029472.2:n.48-50T=
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