Canonical Allele Identifier: CA347679595
Gene: SNRNP200 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.96293097T>A , CM000664.2:g.96293097T>A GRCh38
NC_000002.11:g.96958835T>A , CM000664.1:g.96958835T>A GRCh37
NC_000002.10:g.96322562T>A NCBI36
NG_016973.1:g.17463A>T

Transcript Alleles

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