Canonical Allele Identifier: CA52399730
Gene: SNRNP200 HGNC NCBI

Linked Data

dbSNP Id: rs899315996
MyVariant Identifiers: chr2:g.96958684A>C (hg19) chr2:g.96292946A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.96292946A>C , CM000664.2:g.96292946A>C GRCh38
NC_000002.11:g.96958684A>C , CM000664.1:g.96958684A>C GRCh37
NC_000002.10:g.96322411A>C NCBI36
NG_016973.1:g.17614T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000323853.10:c.2160+26T>G MANE Select ENSP00000317123.5:n.2160+26T>G
ENST00000652267.1:c.2160+26T>G ENSP00000498933.1:n.2160+26T>G
ENST00000323853.9:c.2160+26T>G ENSP00000317123.5:n.2160+26T>G
NM_014014.4:c.2160+26T>G NP_054733.2:n.2160+26T>G
NM_014014.5:c.2160+26T>G MANE Select NP_054733.2:n.2160+26T>G
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