Canonical Allele Identifier: CA1272543506
Gene: SNRNP200 HGNC NCBI

Linked Data

dbSNP Id: rs1320648021
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.96293099G>A , CM000664.2:g.96293099G>A GRCh38
NC_000002.11:g.96958837G>A , CM000664.1:g.96958837G>A GRCh37
NC_000002.10:g.96322564G>A NCBI36
NG_016973.1:g.17461C>T

Transcript Alleles

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