Canonical Allele Identifier: CA1381557999
Gene: CHMP2B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.87253391C= , CM000665.2:g.87253391C= GRCh38
NC_000003.11:g.87302541C= , CM000665.1:g.87302541C= GRCh37
NC_000003.10:g.87385231C= NCBI36
NG_007885.1:g.31129C=

Transcript Alleles

HGVS Amino-acid change
ENST00000263780.9:c.425-13C= MANE Select ENSP00000263780.4:n.425-13C=
ENST00000472024.3:c.473-13C= ENSP00000480032.2:n.473-13C=
ENST00000676705.1:c.473-13C= ENSP00000504098.1:n.473-13C=
ENST00000677929.1:n.4076C=
ENST00000678859.1:n.4161C=
ENST00000263780.8:c.425-13C= ENSP00000263780.4:n.425-13C=
ENST00000466696.1:n.343C=
ENST00000471660.5:c.302-13C= ENSP00000419998.1:n.302-13C=
ENST00000472024.2:c.473-13C= ENSP00000480032.1:n.473-13C=
ENST00000494980.5:c.335-13C= ENSP00000418920.1:n.335-13C=
NM_001244644.1:c.302-13C= NP_001231573.1:n.302-13C=
NM_014043.3:c.425-13C= NP_054762.2:n.425-13C=
XM_011533576.1:c.473-13C= XP_011531878.1:n.473-13C=
XM_011533576.2:c.473-13C= XP_011531878.1:n.473-13C=
NM_014043.4:c.425-13C= MANE Select NP_054762.2:n.425-13C=
NM_001244644.2:c.302-13C= NP_001231573.1:n.302-13C=