Canonical Allele Identifier: CA475201944

Gene: IGHMBP2

Linked Data

• MyVariant Identifiers: chr11:g.68701548T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68934080T>A , CM000673.2:g.68934080T>A	GRCh38
NC_000011.9:g.68701548T>A , CM000673.1:g.68701548T>A	GRCh37
NC_000011.8:g.68458124T>A	NCBI36
NG_007976.1:g.35230T>A , LRG_250:g.35230T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000255078.8:c.1537+167T>A MANE Select	ENSP00000255078.4:n.1537+167T>A
ENST00000674955.1:c.*254+167T>A	ENSP00000502463.1:n.*254+167T>A
ENST00000675118.1:c.1025+167T>A
ENST00000675205.1:n.184-384T>A
ENST00000675615.1:c.1537+167T>A	ENSP00000502413.1:n.1537+167T>A
ENST00000675648.1:n.912+167T>A
ENST00000675997.1:n.113-384T>A
ENST00000676173.1:n.2282+167T>A
ENST00000676228.1:c.*860+167T>A	ENSP00000502375.1:n.*860+167T>A
ENST00000255078.7:c.1537+167T>A	ENSP00000255078.3:n.1537+167T>A
ENST00000539064.5:n.1296+167T>A
ENST00000541229.5:n.232+167T>A
ENST00000543739.5:n.654+167T>A
NM_002180.2:c.1537+167T>A , LRG_250t1:c.1537+167T>A	NP_002171.2:n.1537+167T>A
XM_005273974.2:c.526+167T>A	XP_005274031.1:n.526+167T>A
XM_005273975.2:c.409+167T>A	XP_005274032.1:n.409+167T>A
XM_011544994.1:c.304+167T>A	XP_011543296.1:n.304+167T>A
XR_949903.1:n.1639+167T>A
XM_005273975.3:c.409+167T>A	XP_005274032.1:n.409+167T>A
XM_017017669.2:c.526+167T>A	XP_016873158.1:n.526+167T>A
XM_017017670.2:c.526+167T>A	XP_016873159.1:n.526+167T>A
XM_017017671.2:c.1537+167T>A	XP_016873160.1:n.1537+167T>A
XR_949903.3:n.1635+167T>A
NM_002180.3:c.1537+167T>A MANE Select	NP_002171.2:n.1537+167T>A