Canonical Allele Identifier: CA2666628593

Gene: CHMP2B

Linked Data

• gnomAD v4: 3-87253401-T-TAG

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.87253402_87253403dup , CM000665.2:g.87253402_87253403dup	GRCh38
NC_000003.11:g.87302552_87302553dup , CM000665.1:g.87302552_87302553dup	GRCh37
NC_000003.10:g.87385242_87385243dup	NCBI36
NG_007885.1:g.31140_31141dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000263780.9:c.425-2_425-1dup MANE Select	ENSP00000263780.4:n.425-2_425-1dup
ENST00000472024.3:c.473-2_473-1dup	ENSP00000480032.2:n.473-2_473-1dup
ENST00000676705.1:c.473-2_473-1dup	ENSP00000504098.1:n.473-2_473-1dup
ENST00000677929.1:n.4087_4088dup
ENST00000678859.1:n.4172_4173dup
ENST00000263780.8:c.425-2_425-1dup	ENSP00000263780.4:n.425-2_425-1dup
ENST00000466696.1:n.354_355dup
ENST00000471660.5:c.302-2_302-1dup	ENSP00000419998.1:n.302-2_302-1dup
ENST00000472024.2:c.473-2_473-1dup	ENSP00000480032.1:n.473-2_473-1dup
ENST00000494980.5:c.335-2_335-1dup	ENSP00000418920.1:n.335-2_335-1dup
NM_001244644.1:c.302-2_302-1dup	NP_001231573.1:n.302-2_302-1dup
NM_014043.3:c.425-2_425-1dup	NP_054762.2:n.425-2_425-1dup
XM_011533576.1:c.473-2_473-1dup	XP_011531878.1:n.473-2_473-1dup
XM_011533576.2:c.473-2_473-1dup	XP_011531878.1:n.473-2_473-1dup
NM_014043.4:c.425-2_425-1dup MANE Select	NP_054762.2:n.425-2_425-1dup
NM_001244644.2:c.302-2_302-1dup	NP_001231573.1:n.302-2_302-1dup