Canonical Allele Identifier: CA353696938

Gene: CHMP2B

Linked Data

• MyVariant Identifiers: chr3:g.87294954A>T (hg19) ; chr3:g.87245804A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.87245804A>T , CM000665.2:g.87245804A>T	GRCh38
NC_000003.11:g.87294954A>T , CM000665.1:g.87294954A>T	GRCh37
NC_000003.10:g.87377644A>T	NCBI36
NG_007885.1:g.23542A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000263780.9:c.217A>T MANE Select	ENSP00000263780.4:p.Thr73Ser
ENST00000472024.3:c.265A>T	ENSP00000480032.2:p.Thr89Ser
ENST00000676705.1:c.265A>T	ENSP00000504098.1:p.Thr89Ser
ENST00000676947.1:n.370A>T
ENST00000677929.1:n.455A>T
ENST00000678818.1:n.1063-611A>T
ENST00000678859.1:n.540A>T
ENST00000263780.8:c.217A>T	ENSP00000263780.4:p.Thr73Ser
ENST00000471660.5:c.94A>T	ENSP00000419998.1:p.Thr32Ser
ENST00000472024.2:c.265A>T	ENSP00000480032.1:p.Thr89Ser
ENST00000494980.5:c.217A>T	ENSP00000418920.1:p.Thr73Ser
NM_001244644.1:c.94A>T	NP_001231573.1:p.Thr32Ser
NM_014043.3:c.217A>T	NP_054762.2:p.Thr73Ser
XM_011533576.1:c.265A>T	XP_011531878.1:p.Thr89Ser
XM_011533576.2:c.265A>T	XP_011531878.1:p.Thr89Ser
NM_014043.4:c.217A>T MANE Select	NP_054762.2:p.Thr73Ser
NM_001244644.2:c.94A>T	NP_001231573.1:p.Thr32Ser