Canonical Allele Identifier: CA381653862

Gene: IGHMBP2

Linked Data

• MyVariant Identifiers: chr11:g.68704475A>T (hg19) ; chr11:g.68937007A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68937007A>T , CM000673.2:g.68937007A>T	GRCh38
NC_000011.9:g.68704475A>T , CM000673.1:g.68704475A>T	GRCh37
NC_000011.8:g.68461051A>T	NCBI36
NG_007976.1:g.38157A>T , LRG_250:g.38157A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000255078.8:c.2527A>T MANE Select	ENSP00000255078.4:p.Ser843Cys
ENST00000674675.1:c.672A>T
ENST00000674878.1:c.632A>T
ENST00000675118.1:c.2015A>T
ENST00000675389.1:n.802A>T
ENST00000675615.1:c.2527A>T	ENSP00000502413.1:p.Ser843Cys
ENST00000675648.1:n.1902A>T
ENST00000675916.1:c.771A>T
ENST00000676173.1:n.3272A>T
ENST00000676182.1:c.958A>T
ENST00000676228.1:c.*1850A>T	ENSP00000502375.1:n.*1850A>T
ENST00000255078.7:c.2527A>T	ENSP00000255078.3:p.Ser843Cys
ENST00000539064.5:n.2286A>T
ENST00000543739.5:n.1520A>T
NM_002180.2:c.2527A>T , LRG_250t1:c.2527A>T	NP_002171.2:p.Ser843Cys
XM_005273974.2:c.1516A>T	XP_005274031.1:p.Ser506Cys
XM_005273975.2:c.1399A>T	XP_005274032.1:p.Ser467Cys
XM_011544994.1:c.1294A>T	XP_011543296.1:p.Ser432Cys
XR_949903.1:n.2629A>T
XM_005273975.3:c.1399A>T	XP_005274032.1:p.Ser467Cys
XM_017017669.2:c.1516A>T	XP_016873158.1:p.Ser506Cys
XM_017017670.2:c.1516A>T	XP_016873159.1:p.Ser506Cys
XR_949903.3:n.2625A>T
NM_002180.3:c.2527A>T MANE Select	NP_002171.2:p.Ser843Cys