Canonical Allele Identifier: CA895728792
Gene: SNRNP200 HGNC NCBI

Linked Data

dbSNP Id: rs1400850166
gnomAD v4: 2-96293128-T-C
MyVariant Identifiers: chr2:g.96958866T>C (hg19) chr2:g.96293128T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.96293128T>C , CM000664.2:g.96293128T>C GRCh38
NC_000002.11:g.96958866T>C , CM000664.1:g.96958866T>C GRCh37
NC_000002.10:g.96322593T>C NCBI36
NG_016973.1:g.17432A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000323853.10:c.2037-33A>G MANE Select ENSP00000317123.5:n.2037-33A>G
ENST00000652267.1:c.2037-33A>G ENSP00000498933.1:n.2037-33A>G
ENST00000323853.9:c.2037-33A>G ENSP00000317123.5:n.2037-33A>G
NM_014014.4:c.2037-33A>G NP_054733.2:n.2037-33A>G
NM_014014.5:c.2037-33A>G MANE Select NP_054733.2:n.2037-33A>G
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