Canonical Allele Identifier: CA408016101

Gene: SNRPB

Linked Data

• MyVariant Identifiers: chr20:g.2451332A>C (hg19) ; chr20:g.2470686A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.2470686A>C , CM000682.2:g.2470686A>C	GRCh38
NC_000020.10:g.2451332A>C , CM000682.1:g.2451332A>C	GRCh37
NC_000020.9:g.2399332A>C	NCBI36
NG_042057.1:g.5168T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000688423.1:n.100+2T>G
ENST00000688775.1:n.100+2T>G
ENST00000689440.1:n.102+2T>G
ENST00000690623.1:n.52+2T>G
ENST00000693393.1:n.102+2T>G
ENST00000381342.7:c.3+2T>G MANE Select	ENSP00000370746.3:n.3+2T>G
ENST00000339610.10:c.3+2T>G	ENSP00000342305.7:n.3+2T>G
ENST00000381342.6:c.3+2T>G	ENSP00000370746.2:n.3+2T>G
ENST00000438552.6:c.3+2T>G	ENSP00000412566.2:n.3+2T>G
ENST00000461548.1:c.305-2928T>G	ENSP00000456213.1:n.305-2928T>G
ENST00000474384.2:c.3+2T>G	ENSP00000474579.1:n.3+2T>G
NM_003091.3:c.3+2T>G	NP_003082.1:n.3+2T>G
NM_198216.1:c.3+2T>G	NP_937859.1:n.3+2T>G
NM_003091.4:c.3+2T>G MANE Select	NP_003082.1:n.3+2T>G
NM_198216.2:c.3+2T>G	NP_937859.1:n.3+2T>G