Canonical Allele Identifier: CA381651729

Gene: IGHMBP2

Linked Data

• MyVariant Identifiers: chr11:g.68703803A>T (hg19) ; chr11:g.68936335A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68936335A>T , CM000673.2:g.68936335A>T	GRCh38
NC_000011.9:g.68703803A>T , CM000673.1:g.68703803A>T	GRCh37
NC_000011.8:g.68460379A>T	NCBI36
NG_007976.1:g.37485A>T , LRG_250:g.37485A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000255078.8:c.1855A>T MANE Select	ENSP00000255078.4:p.Asn619Tyr
ENST00000674675.1:c.99A>T
ENST00000674878.1:c.99A>T
ENST00000674955.1:c.*572A>T	ENSP00000502463.1:n.*572A>T
ENST00000675118.1:c.1343A>T
ENST00000675389.1:n.130A>T
ENST00000675615.1:c.1855A>T	ENSP00000502413.1:p.Asn619Tyr
ENST00000675648.1:n.1230A>T
ENST00000675916.1:c.99A>T
ENST00000676173.1:n.2600A>T
ENST00000676182.1:c.286A>T
ENST00000676228.1:c.*1178A>T	ENSP00000502375.1:n.*1178A>T
ENST00000255078.7:c.1855A>T	ENSP00000255078.3:p.Asn619Tyr
ENST00000539064.5:n.1614A>T
ENST00000543739.5:n.848A>T
ENST00000545475.1:n.451A>T
NM_002180.2:c.1855A>T , LRG_250t1:c.1855A>T	NP_002171.2:p.Asn619Tyr
XM_005273974.2:c.844A>T	XP_005274031.1:p.Asn282Tyr
XM_005273975.2:c.727A>T	XP_005274032.1:p.Asn243Tyr
XM_011544994.1:c.622A>T	XP_011543296.1:p.Asn208Tyr
XR_949903.1:n.1957A>T
XM_005273975.3:c.727A>T	XP_005274032.1:p.Asn243Tyr
XM_017017669.2:c.844A>T	XP_016873158.1:p.Asn282Tyr
XM_017017670.2:c.844A>T	XP_016873159.1:p.Asn282Tyr
XR_949903.3:n.1953A>T
NM_002180.3:c.1855A>T MANE Select	NP_002171.2:p.Asn619Tyr