Canonical Allele Identifier: CA9732391
Gene: SNRPB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.2462717G>A , CM000682.2:g.2462717G>A GRCh38
NC_000020.10:g.2443363G>A , CM000682.1:g.2443363G>A GRCh37
NC_000020.9:g.2391363G>A NCBI36
NG_042057.1:g.13137C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000688423.1:n.3007C>T
ENST00000688450.1:n.1684C>T
ENST00000688775.1:n.2488C>T
ENST00000689440.1:n.2199C>T
ENST00000689611.1:n.1853C>T
ENST00000690623.1:n.777C>T
ENST00000693393.1:n.2490C>T
ENST00000381342.7:c.604C>T MANE Select ENSP00000370746.3:p.Pro202Ser
ENST00000339610.10:c.604C>T ENSP00000342305.7:p.Pro202Ser
ENST00000381342.6:c.604C>T ENSP00000370746.2:p.Pro202Ser
ENST00000438552.6:c.604C>T ENSP00000412566.2:p.Pro202Ser
ENST00000474384.2:c.*515C>T ENSP00000474579.1:n.*515C>T
NM_003091.3:c.604C>T NP_003082.1:p.Pro202Ser
NM_198216.1:c.604C>T NP_937859.1:p.Pro202Ser
NM_003091.4:c.604C>T MANE Select NP_003082.1:p.Pro202Ser
NM_198216.2:c.604C>T NP_937859.1:p.Pro202Ser