Canonical Allele Identifier: CA1272543450

Gene: SNRNP200

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.96292934G= , CM000664.2:g.96292934G=	GRCh38
NC_000002.11:g.96958672G= , CM000664.1:g.96958672G=	GRCh37
NC_000002.10:g.96322399G=	NCBI36
NG_016973.1:g.17626C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000323853.10:c.2160+38C= MANE Select	ENSP00000317123.5:n.2160+38C=
ENST00000652267.1:c.2160+38C=	ENSP00000498933.1:n.2160+38C=
ENST00000323853.9:c.2160+38C=	ENSP00000317123.5:n.2160+38C=
NM_014014.4:c.2160+38C=	NP_054733.2:n.2160+38C=
NM_014014.5:c.2160+38C= MANE Select	NP_054733.2:n.2160+38C=