Canonical Allele Identifier: CA79035829

Gene: CHMP2B

Linked Data

• dbSNP Id: rs139070624
• gnomAD v3: 3-87254479-G-T
• gnomAD v4: 3-87254479-G-T
• MyVariant Identifiers: chr3:g.87303629G>T (hg19) ; chr3:g.87254479G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.87254479G>T , CM000665.2:g.87254479G>T	GRCh38
NC_000003.11:g.87303629G>T , CM000665.1:g.87303629G>T	GRCh37
NC_000003.10:g.87386319G>T	NCBI36
NG_007885.1:g.32217G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263780.9:c.*657G>T MANE Select	ENSP00000263780.4:n.*657G>T
ENST00000472024.3:c.*657G>T	ENSP00000480032.2:n.*657G>T
ENST00000676705.1:c.*657G>T	ENSP00000504098.1:n.*657G>T
ENST00000677929.1:n.4963G>T
ENST00000678859.1:n.5048G>T
ENST00000263780.8:c.*657G>T	ENSP00000263780.4:n.*657G>T
ENST00000471660.5:c.*657G>T	ENSP00000419998.1:n.*657G>T
NM_001244644.1:c.*657G>T	NP_001231573.1:n.*657G>T
NM_014043.3:c.*657G>T	NP_054762.2:n.*657G>T
XM_011533576.1:c.*657G>T	XP_011531878.1:n.*657G>T
XM_011533576.2:c.*657G>T	XP_011531878.1:n.*657G>T
NM_014043.4:c.*657G>T MANE Select	NP_054762.2:n.*657G>T
NM_001244644.2:c.*657G>T	NP_001231573.1:n.*657G>T