Canonical Allele Identifier: CA1381558036
Gene: CHMP2B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.87253424A= , CM000665.2:g.87253424A= GRCh38
NC_000003.11:g.87302574A= , CM000665.1:g.87302574A= GRCh37
NC_000003.10:g.87385264A= NCBI36
NG_007885.1:g.31162A=

Transcript Alleles

HGVS Amino-acid change
ENST00000263780.9:c.445A= MANE Select ENSP00000263780.4:p.Ile149=
ENST00000472024.3:c.493A= ENSP00000480032.2:p.Ile165=
ENST00000676705.1:c.493A= ENSP00000504098.1:p.Ile165=
ENST00000677929.1:n.4109A=
ENST00000678859.1:n.4194A=
ENST00000263780.8:c.445A= ENSP00000263780.4:p.Ile149=
ENST00000466696.1:n.376A=
ENST00000471660.5:c.322A= ENSP00000419998.1:p.Ile108=
ENST00000472024.2:c.493A= ENSP00000480032.1:p.Ile165=
ENST00000494980.5:c.355A= ENSP00000418920.1:p.Ile119=
NM_001244644.1:c.322A= NP_001231573.1:p.Ile108=
NM_014043.3:c.445A= NP_054762.2:p.Ile149=
XM_011533576.1:c.493A= XP_011531878.1:p.Ile165=
XM_011533576.2:c.493A= XP_011531878.1:p.Ile165=
NM_014043.4:c.445A= MANE Select NP_054762.2:p.Ile149=
NM_001244644.2:c.322A= NP_001231573.1:p.Ile108=