Canonical Allele Identifier: CA2699990168

Gene: SNRNP200

Linked Data

• dbSNP Id: rs2104352226

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.96293191del , CM000664.2:g.96293191del	GRCh38
NC_000002.11:g.96958929del , CM000664.1:g.96958929del	GRCh37
NC_000002.10:g.96322656del	NCBI36
NG_016973.1:g.17371del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000323853.10:c.2037-94del MANE Select	ENSP00000317123.5:n.2037-94del
ENST00000652267.1:c.2037-94del	ENSP00000498933.1:n.2037-94del
ENST00000323853.9:c.2037-94del	ENSP00000317123.5:n.2037-94del
NM_014014.4:c.2037-94del	NP_054733.2:n.2037-94del
NM_014014.5:c.2037-94del MANE Select	NP_054733.2:n.2037-94del