Canonical Allele Identifier: CA353696947

Gene: CHMP2B

Linked Data

• MyVariant Identifiers: chr3:g.87294959A>C (hg19) ; chr3:g.87245809A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.87245809A>C , CM000665.2:g.87245809A>C	GRCh38
NC_000003.11:g.87294959A>C , CM000665.1:g.87294959A>C	GRCh37
NC_000003.10:g.87377649A>C	NCBI36
NG_007885.1:g.23547A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000263780.9:c.222A>C MANE Select	ENSP00000263780.4:p.Arg74Ser
ENST00000472024.3:c.270A>C	ENSP00000480032.2:p.Arg90Ser
ENST00000676705.1:c.270A>C	ENSP00000504098.1:p.Arg90Ser
ENST00000676947.1:n.375A>C
ENST00000677929.1:n.460A>C
ENST00000678818.1:n.1063-606A>C
ENST00000678859.1:n.545A>C
ENST00000263780.8:c.222A>C	ENSP00000263780.4:p.Arg74Ser
ENST00000471660.5:c.99A>C	ENSP00000419998.1:p.Arg33Ser
ENST00000472024.2:c.270A>C	ENSP00000480032.1:p.Arg90Ser
ENST00000494980.5:c.222A>C	ENSP00000418920.1:p.Arg74Ser
NM_001244644.1:c.99A>C	NP_001231573.1:p.Arg33Ser
NM_014043.3:c.222A>C	NP_054762.2:p.Arg74Ser
XM_011533576.1:c.270A>C	XP_011531878.1:p.Arg90Ser
XM_011533576.2:c.270A>C	XP_011531878.1:p.Arg90Ser
NM_014043.4:c.222A>C MANE Select	NP_054762.2:p.Arg74Ser
NM_001244644.2:c.99A>C	NP_001231573.1:p.Arg33Ser