Canonical Allele Identifier: CA911571096
Gene: CHMP2B HGNC NCBI

Linked Data

dbSNP Id: rs1426978593

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.87253280dup , CM000665.2:g.87253280dup GRCh38
NC_000003.11:g.87302430dup , CM000665.1:g.87302430dup GRCh37
NC_000003.10:g.87385120dup NCBI36
NG_007885.1:g.31018dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000263780.9:c.425-124dup MANE Select ENSP00000263780.4:n.425-124dup
ENST00000472024.3:c.473-124dup ENSP00000480032.2:n.473-124dup
ENST00000676705.1:c.473-124dup ENSP00000504098.1:n.473-124dup
ENST00000677929.1:n.3965dup
ENST00000678859.1:n.4050dup
ENST00000263780.8:c.425-124dup ENSP00000263780.4:n.425-124dup
ENST00000466696.1:n.232dup
ENST00000471660.5:c.302-124dup ENSP00000419998.1:n.302-124dup
ENST00000472024.2:c.473-124dup ENSP00000480032.1:n.473-124dup
ENST00000494980.5:c.335-124dup ENSP00000418920.1:n.335-124dup
NM_001244644.1:c.302-124dup NP_001231573.1:n.302-124dup
NM_014043.3:c.425-124dup NP_054762.2:n.425-124dup
XM_011533576.1:c.473-124dup XP_011531878.1:n.473-124dup
XM_011533576.2:c.473-124dup XP_011531878.1:n.473-124dup
NM_014043.4:c.425-124dup MANE Select NP_054762.2:n.425-124dup
NM_001244644.2:c.302-124dup NP_001231573.1:n.302-124dup