Canonical Allele Identifier: CA1272543430
Gene: SNRNP200 HGNC NCBI

Linked Data

dbSNP Id: rs2063892394

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.96292891dup , CM000664.2:g.96292891dup GRCh38
NC_000002.11:g.96958629dup , CM000664.1:g.96958629dup GRCh37
NC_000002.10:g.96322356dup NCBI36
NG_016973.1:g.17671dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000323853.10:c.2160+83dup MANE Select ENSP00000317123.5:n.2160+83dup
ENST00000652267.1:c.2160+83dup ENSP00000498933.1:n.2160+83dup
ENST00000323853.9:c.2160+83dup ENSP00000317123.5:n.2160+83dup
NM_014014.4:c.2160+83dup NP_054733.2:n.2160+83dup
NM_014014.5:c.2160+83dup MANE Select NP_054733.2:n.2160+83dup