Canonical Allele Identifier: CA353697492

Gene: CHMP2B

Linked Data

• gnomAD v4: 3-87253424-A-C
• MyVariant Identifiers: chr3:g.87302574A>C (hg19) ; chr3:g.87253424A>C (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid change
ENST00000263780.9:c.445A>C MANE Select	ENSP00000263780.4:p.Ile149Leu
ENST00000472024.3:c.493A>C	ENSP00000480032.2:p.Ile165Leu
ENST00000676705.1:c.493A>C	ENSP00000504098.1:p.Ile165Leu
ENST00000677929.1:n.4109A>C
ENST00000678859.1:n.4194A>C
ENST00000263780.8:c.445A>C	ENSP00000263780.4:p.Ile149Leu
ENST00000466696.1:n.376A>C
ENST00000471660.5:c.322A>C	ENSP00000419998.1:p.Ile108Leu
ENST00000472024.2:c.493A>C	ENSP00000480032.1:p.Ile165Leu
ENST00000494980.5:c.355A>C	ENSP00000418920.1:p.Ile119Leu
NM_001244644.1:c.322A>C	NP_001231573.1:p.Ile108Leu
NM_014043.3:c.445A>C	NP_054762.2:p.Ile149Leu
XM_011533576.1:c.493A>C	XP_011531878.1:p.Ile165Leu
XM_011533576.2:c.493A>C	XP_011531878.1:p.Ile165Leu
NM_014043.4:c.445A>C MANE Select	NP_054762.2:p.Ile149Leu
NM_001244644.2:c.322A>C	NP_001231573.1:p.Ile108Leu