Canonical Allele Identifier: CA347679588
Gene: SNRNP200 HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.96958834C>T (hg19) chr2:g.96293096C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.96293096C>T , CM000664.2:g.96293096C>T GRCh38
NC_000002.11:g.96958834C>T , CM000664.1:g.96958834C>T GRCh37
NC_000002.10:g.96322561C>T NCBI36
NG_016973.1:g.17464G>A

Transcript Alleles

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