Canonical Allele Identifier: CA1381558038
Gene: CHMP2B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.87253432C= , CM000665.2:g.87253432C= GRCh38
NC_000003.11:g.87302582C= , CM000665.1:g.87302582C= GRCh37
NC_000003.10:g.87385272C= NCBI36
NG_007885.1:g.31170C=

Transcript Alleles

HGVS Amino-acid change
ENST00000263780.9:c.453C= MANE Select ENSP00000263780.4:p.Asp151=
ENST00000472024.3:c.501C= ENSP00000480032.2:p.Asp167=
ENST00000676705.1:c.501C= ENSP00000504098.1:p.Asp167=
ENST00000677929.1:n.4117C=
ENST00000678859.1:n.4202C=
ENST00000263780.8:c.453C= ENSP00000263780.4:p.Asp151=
ENST00000466696.1:n.384C=
ENST00000471660.5:c.330C= ENSP00000419998.1:p.Asp110=
ENST00000472024.2:c.501C= ENSP00000480032.1:p.Asp167=
ENST00000494980.5:c.363C= ENSP00000418920.1:p.Asp121=
NM_001244644.1:c.330C= NP_001231573.1:p.Asp110=
NM_014043.3:c.453C= NP_054762.2:p.Asp151=
XM_011533576.1:c.501C= XP_011531878.1:p.Asp167=
XM_011533576.2:c.501C= XP_011531878.1:p.Asp167=
NM_014043.4:c.453C= MANE Select NP_054762.2:p.Asp151=
NM_001244644.2:c.330C= NP_001231573.1:p.Asp110=