Canonical Allele Identifier: CA742353469

Gene: SNRPB

Linked Data

• dbSNP Id: rs987618381
• MyVariant Identifiers: chr20:g.2451485A>T (hg19) ; chr20:g.2470839A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.2470839A>T , CM000682.2:g.2470839A>T	GRCh38
NC_000020.10:g.2451485A>T , CM000682.1:g.2451485A>T	GRCh37
NC_000020.9:g.2399485A>T	NCBI36
NG_042057.1:g.5015T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000381342.6:c.-149T>A	ENSP00000370746.2:n.-149T>A
ENST00000438552.6:c.-149T>A	ENSP00000412566.2:n.-149T>A
ENST00000461548.1:c.305-3081T>A	ENSP00000456213.1:n.305-3081T>A
NM_003091.3:c.-149T>A	NP_003082.1:n.-149T>A
NM_198216.1:c.-149T>A	NP_937859.1:n.-149T>A