Canonical Allele Identifier: CA2660185978

Gene: SNRNP200

Linked Data

• gnomAD v4: 2-96292864-T-TGG

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.96292864_96292865insGG , CM000664.2:g.96292864_96292865insGG	GRCh38
NC_000002.11:g.96958602_96958603insGG , CM000664.1:g.96958602_96958603insGG	GRCh37
NC_000002.10:g.96322329_96322330insGG	NCBI36
NG_016973.1:g.17695_17696insCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000323853.10:c.2160+107_2160+108insCC MANE Select	ENSP00000317123.5:n.2160+107_2160+108insCC
ENST00000652267.1:c.2160+107_2160+108insCC	ENSP00000498933.1:n.2160+107_2160+108insCC
ENST00000323853.9:c.2160+107_2160+108insCC	ENSP00000317123.5:n.2160+107_2160+108insCC
NM_014014.4:c.2160+107_2160+108insCC	NP_054733.2:n.2160+107_2160+108insCC
NM_014014.5:c.2160+107_2160+108insCC MANE Select	NP_054733.2:n.2160+107_2160+108insCC