Canonical Allele Identifier: CA1381558041
Gene: CHMP2B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.87253433G= , CM000665.2:g.87253433G= GRCh38
NC_000003.11:g.87302583G= , CM000665.1:g.87302583G= GRCh37
NC_000003.10:g.87385273G= NCBI36
NG_007885.1:g.31171G=

Transcript Alleles

HGVS Amino-acid change
ENST00000263780.9:c.454G= MANE Select ENSP00000263780.4:p.Gly152=
ENST00000472024.3:c.502G= ENSP00000480032.2:p.Gly168=
ENST00000676705.1:c.502G= ENSP00000504098.1:p.Gly168=
ENST00000677929.1:n.4118G=
ENST00000678859.1:n.4203G=
ENST00000263780.8:c.454G= ENSP00000263780.4:p.Gly152=
ENST00000466696.1:n.385G=
ENST00000471660.5:c.331G= ENSP00000419998.1:p.Gly111=
ENST00000472024.2:c.502G= ENSP00000480032.1:p.Gly168=
ENST00000494980.5:c.364G= ENSP00000418920.1:p.Gly122=
NM_001244644.1:c.331G= NP_001231573.1:p.Gly111=
NM_014043.3:c.454G= NP_054762.2:p.Gly152=
XM_011533576.1:c.502G= XP_011531878.1:p.Gly168=
XM_011533576.2:c.502G= XP_011531878.1:p.Gly168=
NM_014043.4:c.454G= MANE Select NP_054762.2:p.Gly152=
NM_001244644.2:c.331G= NP_001231573.1:p.Gly111=