Canonical Allele Identifier: CA2577827033
Gene: CHMP2B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.87253402del , CM000665.2:g.87253402del GRCh38
NC_000003.11:g.87302552del , CM000665.1:g.87302552del GRCh37
NC_000003.10:g.87385242del NCBI36
NG_007885.1:g.31140del

Transcript Alleles

HGVS Amino-acid change
ENST00000263780.9:c.425-2del MANE Select ENSP00000263780.4:n.425-2del
ENST00000472024.3:c.473-2del ENSP00000480032.2:n.473-2del
ENST00000676705.1:c.473-2del ENSP00000504098.1:n.473-2del
ENST00000677929.1:n.4087del
ENST00000678859.1:n.4172del
ENST00000263780.8:c.425-2del ENSP00000263780.4:n.425-2del
ENST00000466696.1:n.354del
ENST00000471660.5:c.302-2del ENSP00000419998.1:n.302-2del
ENST00000472024.2:c.473-2del ENSP00000480032.1:n.473-2del
ENST00000494980.5:c.335-2del ENSP00000418920.1:n.335-2del
NM_001244644.1:c.302-2del NP_001231573.1:n.302-2del
NM_014043.3:c.425-2del NP_054762.2:n.425-2del
XM_011533576.1:c.473-2del XP_011531878.1:n.473-2del
XM_011533576.2:c.473-2del XP_011531878.1:n.473-2del
NM_014043.4:c.425-2del MANE Select NP_054762.2:n.425-2del
NM_001244644.2:c.302-2del NP_001231573.1:n.302-2del