Canonical Allele Identifier: CA1272543465
Gene: SNRNP200 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.96292976T= , CM000664.2:g.96292976T= GRCh38
NC_000002.11:g.96958714T= , CM000664.1:g.96958714T= GRCh37
NC_000002.10:g.96322441T= NCBI36
NG_016973.1:g.17584A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000323853.10:c.2156A= MANE Select ENSP00000317123.5:p.Asn719=
ENST00000652267.1:c.2156A= ENSP00000498933.1:p.Asn719=
ENST00000323853.9:c.2156A= ENSP00000317123.5:p.Asn719=
NM_014014.4:c.2156A= NP_054733.2:p.Asn719=
NM_014014.5:c.2156A= MANE Select NP_054733.2:p.Asn719=
Search 100 bp 5'
Search 100 bp 3'