Canonical Allele Identifier: CA2660186209

Gene: SNRNP200

Linked Data

• gnomAD v4: 2-96293183-T-A

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.96293183T>A , CM000664.2:g.96293183T>A	GRCh38
NC_000002.11:g.96958921T>A , CM000664.1:g.96958921T>A	GRCh37
NC_000002.10:g.96322648T>A	NCBI36
NG_016973.1:g.17377A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000323853.10:c.2037-88A>T MANE Select	ENSP00000317123.5:n.2037-88A>T
ENST00000652267.1:c.2037-88A>T	ENSP00000498933.1:n.2037-88A>T
ENST00000323853.9:c.2037-88A>T	ENSP00000317123.5:n.2037-88A>T
NM_014014.4:c.2037-88A>T	NP_054733.2:n.2037-88A>T
NM_014014.5:c.2037-88A>T MANE Select	NP_054733.2:n.2037-88A>T