Canonical Allele Identifier: CA1381557905

Gene: CHMP2B

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.87253242T= , CM000665.2:g.87253242T=	GRCh38
NC_000003.11:g.87302392T= , CM000665.1:g.87302392T=	GRCh37
NC_000003.10:g.87385082T=	NCBI36
NG_007885.1:g.30980T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263780.9:c.425-162T= MANE Select	ENSP00000263780.4:n.425-162T=
ENST00000472024.3:c.473-162T=	ENSP00000480032.2:n.473-162T=
ENST00000676705.1:c.473-162T=	ENSP00000504098.1:n.473-162T=
ENST00000677929.1:n.3927T=
ENST00000678859.1:n.4012T=
ENST00000263780.8:c.425-162T=	ENSP00000263780.4:n.425-162T=
ENST00000466696.1:n.194T=
ENST00000471660.5:c.302-162T=	ENSP00000419998.1:n.302-162T=
ENST00000472024.2:c.473-162T=	ENSP00000480032.1:n.473-162T=
ENST00000494980.5:c.335-162T=	ENSP00000418920.1:n.335-162T=
NM_001244644.1:c.302-162T=	NP_001231573.1:n.302-162T=
NM_014043.3:c.425-162T=	NP_054762.2:n.425-162T=
XM_011533576.1:c.473-162T=	XP_011531878.1:n.473-162T=
XM_011533576.2:c.473-162T=	XP_011531878.1:n.473-162T=
NM_014043.4:c.425-162T= MANE Select	NP_054762.2:n.425-162T=
NM_001244644.2:c.302-162T=	NP_001231573.1:n.302-162T=