Canonical Allele Identifier: CA381653788

Gene: IGHMBP2

Linked Data

• MyVariant Identifiers: chr11:g.68704448C>A (hg19) ; chr11:g.68936980C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68936980C>A , CM000673.2:g.68936980C>A	GRCh38
NC_000011.9:g.68704448C>A , CM000673.1:g.68704448C>A	GRCh37
NC_000011.8:g.68461024C>A	NCBI36
NG_007976.1:g.38130C>A , LRG_250:g.38130C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000255078.8:c.2500C>A MANE Select	ENSP00000255078.4:p.His834Asn
ENST00000674675.1:c.645C>A
ENST00000674878.1:c.605C>A
ENST00000675118.1:c.1988C>A
ENST00000675389.1:n.775C>A
ENST00000675615.1:c.2500C>A	ENSP00000502413.1:p.His834Asn
ENST00000675648.1:n.1875C>A
ENST00000675916.1:c.744C>A
ENST00000676173.1:n.3245C>A
ENST00000676182.1:c.931C>A
ENST00000676228.1:c.*1823C>A	ENSP00000502375.1:n.*1823C>A
ENST00000255078.7:c.2500C>A	ENSP00000255078.3:p.His834Asn
ENST00000539064.5:n.2259C>A
ENST00000543739.5:n.1493C>A
NM_002180.2:c.2500C>A , LRG_250t1:c.2500C>A	NP_002171.2:p.His834Asn
XM_005273974.2:c.1489C>A	XP_005274031.1:p.His497Asn
XM_005273975.2:c.1372C>A	XP_005274032.1:p.His458Asn
XM_011544994.1:c.1267C>A	XP_011543296.1:p.His423Asn
XR_949903.1:n.2602C>A
XM_005273975.3:c.1372C>A	XP_005274032.1:p.His458Asn
XM_017017669.2:c.1489C>A	XP_016873158.1:p.His497Asn
XM_017017670.2:c.1489C>A	XP_016873159.1:p.His497Asn
XR_949903.3:n.2598C>A
NM_002180.3:c.2500C>A MANE Select	NP_002171.2:p.His834Asn