Canonical Allele Identifier: CA2660185968
Gene: SNRNP200 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.96292850del , CM000664.2:g.96292850del GRCh38
NC_000002.11:g.96958588del , CM000664.1:g.96958588del GRCh37
NC_000002.10:g.96322315del NCBI36
NG_016973.1:g.17710del

Transcript Alleles

HGVS Amino-acid Change
ENST00000323853.10:c.2160+122del MANE Select ENSP00000317123.5:n.2160+122del
ENST00000652267.1:c.2160+122del ENSP00000498933.1:n.2160+122del
ENST00000323853.9:c.2160+122del ENSP00000317123.5:n.2160+122del
NM_014014.4:c.2160+122del NP_054733.2:n.2160+122del
NM_014014.5:c.2160+122del MANE Select NP_054733.2:n.2160+122del