Canonical Allele Identifier: CA347678914
Gene: SNRNP200 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.96292975A>C , CM000664.2:g.96292975A>C GRCh38
NC_000002.11:g.96958713A>C , CM000664.1:g.96958713A>C GRCh37
NC_000002.10:g.96322440A>C NCBI36
NG_016973.1:g.17585T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000323853.10:c.2157T>G MANE Select ENSP00000317123.5:p.Asn719Lys
ENST00000652267.1:c.2157T>G ENSP00000498933.1:p.Asn719Lys
ENST00000323853.9:c.2157T>G ENSP00000317123.5:p.Asn719Lys
NM_014014.4:c.2157T>G NP_054733.2:p.Asn719Lys
NM_014014.5:c.2157T>G MANE Select NP_054733.2:p.Asn719Lys