Canonical Allele Identifier: CA381651544

Gene: IGHMBP2

Linked Data

• MyVariant Identifiers: chr11:g.68703741A>T (hg19) ; chr11:g.68936273A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68936273A>T , CM000673.2:g.68936273A>T	GRCh38
NC_000011.9:g.68703741A>T , CM000673.1:g.68703741A>T	GRCh37
NC_000011.8:g.68460317A>T	NCBI36
NG_007976.1:g.37423A>T , LRG_250:g.37423A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000255078.8:c.1793A>T MANE Select	ENSP00000255078.4:p.Asn598Ile
ENST00000674675.1:c.37A>T
ENST00000674878.1:c.37A>T
ENST00000674955.1:c.*510A>T	ENSP00000502463.1:n.*510A>T
ENST00000675118.1:c.1281A>T
ENST00000675389.1:n.68A>T
ENST00000675615.1:c.1793A>T	ENSP00000502413.1:p.Asn598Ile
ENST00000675648.1:n.1168A>T
ENST00000675916.1:c.37A>T
ENST00000676173.1:n.2538A>T
ENST00000676182.1:c.224A>T
ENST00000676228.1:c.*1116A>T	ENSP00000502375.1:n.*1116A>T
ENST00000255078.7:c.1793A>T	ENSP00000255078.3:p.Asn598Ile
ENST00000539064.5:n.1552A>T
ENST00000541229.5:n.488A>T
ENST00000543739.5:n.786A>T
ENST00000545475.1:n.389A>T
NM_002180.2:c.1793A>T , LRG_250t1:c.1793A>T	NP_002171.2:p.Asn598Ile
XM_005273974.2:c.782A>T	XP_005274031.1:p.Asn261Ile
XM_005273975.2:c.665A>T	XP_005274032.1:p.Asn222Ile
XM_011544994.1:c.560A>T	XP_011543296.1:p.Asn187Ile
XR_949903.1:n.1895A>T
XM_005273975.3:c.665A>T	XP_005274032.1:p.Asn222Ile
XM_017017669.2:c.782A>T	XP_016873158.1:p.Asn261Ile
XM_017017670.2:c.782A>T	XP_016873159.1:p.Asn261Ile
XR_949903.3:n.1891A>T
NM_002180.3:c.1793A>T MANE Select	NP_002171.2:p.Asn598Ile