Canonical Allele Identifier: CA353697485

Gene: CHMP2B

Linked Data

• MyVariant Identifiers: chr3:g.87302571G>A (hg19) ; chr3:g.87253421G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.87253421G>A , CM000665.2:g.87253421G>A	GRCh38
NC_000003.11:g.87302571G>A , CM000665.1:g.87302571G>A	GRCh37
NC_000003.10:g.87385261G>A	NCBI36
NG_007885.1:g.31159G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000263780.9:c.442G>A MANE Select	ENSP00000263780.4:p.Asp148Asn
ENST00000472024.3:c.490G>A	ENSP00000480032.2:p.Asp164Asn
ENST00000676705.1:c.490G>A	ENSP00000504098.1:p.Asp164Asn
ENST00000677929.1:n.4106G>A
ENST00000678859.1:n.4191G>A
ENST00000263780.8:c.442G>A	ENSP00000263780.4:p.Asp148Asn
ENST00000466696.1:n.373G>A
ENST00000471660.5:c.319G>A	ENSP00000419998.1:p.Asp107Asn
ENST00000472024.2:c.490G>A	ENSP00000480032.1:p.Asp164Asn
ENST00000494980.5:c.352G>A	ENSP00000418920.1:p.Asp118Asn
NM_001244644.1:c.319G>A	NP_001231573.1:p.Asp107Asn
NM_014043.3:c.442G>A	NP_054762.2:p.Asp148Asn
XM_011533576.1:c.490G>A	XP_011531878.1:p.Asp164Asn
XM_011533576.2:c.490G>A	XP_011531878.1:p.Asp164Asn
NM_014043.4:c.442G>A MANE Select	NP_054762.2:p.Asp148Asn
NM_001244644.2:c.319G>A	NP_001231573.1:p.Asp107Asn