Canonical Allele Identifier: CA381649580

Gene: IGHMBP2

Linked Data

• MyVariant Identifiers: chr11:g.68701264G>A (hg19) ; chr11:g.68933796G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68933796G>A , CM000673.2:g.68933796G>A	GRCh38
NC_000011.9:g.68701264G>A , CM000673.1:g.68701264G>A	GRCh37
NC_000011.8:g.68457840G>A	NCBI36
NG_007976.1:g.34946G>A , LRG_250:g.34946G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000255078.8:c.1420G>A MANE Select	ENSP00000255078.4:p.Asp474Asn
ENST00000674955.1:c.*137G>A	ENSP00000502463.1:n.*137G>A
ENST00000675118.1:c.908G>A
ENST00000675205.1:n.183+315G>A
ENST00000675615.1:c.1420G>A	ENSP00000502413.1:p.Asp474Asn
ENST00000675648.1:n.795G>A
ENST00000675997.1:n.113-668G>A
ENST00000676173.1:n.2165G>A
ENST00000676228.1:c.*743G>A	ENSP00000502375.1:n.*743G>A
ENST00000255078.7:c.1420G>A	ENSP00000255078.3:p.Asp474Asn
ENST00000537458.5:n.537G>A
ENST00000539064.5:n.1179G>A
ENST00000541229.5:n.115G>A
ENST00000543739.5:n.537G>A
NM_002180.2:c.1420G>A , LRG_250t1:c.1420G>A	NP_002171.2:p.Asp474Asn
XM_005273974.2:c.409G>A	XP_005274031.1:p.Asp137Asn
XM_005273975.2:c.292G>A	XP_005274032.1:p.Asp98Asn
XM_011544994.1:c.187G>A	XP_011543296.1:p.Asp63Asn
XR_949903.1:n.1522G>A
XM_005273975.3:c.292G>A	XP_005274032.1:p.Asp98Asn
XM_017017669.2:c.409G>A	XP_016873158.1:p.Asp137Asn
XM_017017670.2:c.409G>A	XP_016873159.1:p.Asp137Asn
XM_017017671.2:c.1420G>A	XP_016873160.1:p.Asp474Asn
XR_949903.3:n.1518G>A
NM_002180.3:c.1420G>A MANE Select	NP_002171.2:p.Asp474Asn