Canonical Allele Identifier: CA1272543431
Gene: SNRNP200 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.96292894G= , CM000664.2:g.96292894G= GRCh38
NC_000002.11:g.96958632G= , CM000664.1:g.96958632G= GRCh37
NC_000002.10:g.96322359G= NCBI36
NG_016973.1:g.17666C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000323853.10:c.2160+78C= MANE Select ENSP00000317123.5:n.2160+78C=
ENST00000652267.1:c.2160+78C= ENSP00000498933.1:n.2160+78C=
ENST00000323853.9:c.2160+78C= ENSP00000317123.5:n.2160+78C=
NM_014014.4:c.2160+78C= NP_054733.2:n.2160+78C=
NM_014014.5:c.2160+78C= MANE Select NP_054733.2:n.2160+78C=