Canonical Allele Identifier: CA2660186196
Gene: SNRNP200 HGNC NCBI

Linked Data

gnomAD v4: 2-96293140-C-A
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.96293140C>A , CM000664.2:g.96293140C>A GRCh38
NC_000002.11:g.96958878C>A , CM000664.1:g.96958878C>A GRCh37
NC_000002.10:g.96322605C>A NCBI36
NG_016973.1:g.17420G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000323853.10:c.2037-45G>T MANE Select ENSP00000317123.5:n.2037-45G>T
ENST00000652267.1:c.2037-45G>T ENSP00000498933.1:n.2037-45G>T
ENST00000323853.9:c.2037-45G>T ENSP00000317123.5:n.2037-45G>T
NM_014014.4:c.2037-45G>T NP_054733.2:n.2037-45G>T
NM_014014.5:c.2037-45G>T MANE Select NP_054733.2:n.2037-45G>T
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