Canonical Allele Identifier: CA347679550
Gene: SNRNP200 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.96293088G>T , CM000664.2:g.96293088G>T GRCh38
NC_000002.11:g.96958826G>T , CM000664.1:g.96958826G>T GRCh37
NC_000002.10:g.96322553G>T NCBI36
NG_016973.1:g.17472C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000323853.10:c.2044C>A MANE Select ENSP00000317123.5:p.Pro682Thr
ENST00000652267.1:c.2044C>A ENSP00000498933.1:p.Pro682Thr
ENST00000323853.9:c.2044C>A ENSP00000317123.5:p.Pro682Thr
NM_014014.4:c.2044C>A NP_054733.2:p.Pro682Thr
NM_014014.5:c.2044C>A MANE Select NP_054733.2:p.Pro682Thr