Canonical Allele Identifier: CA381644388

Gene: IGHMBP2

Linked Data

• gnomAD v4: 11-68914911-A-T
• MyVariant Identifiers: chr11:g.68682379A>T (hg19) ; chr11:g.68914911A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68914911A>T , CM000673.2:g.68914911A>T	GRCh38
NC_000011.9:g.68682379A>T , CM000673.1:g.68682379A>T	GRCh37
NC_000011.8:g.68438955A>T	NCBI36
NG_007976.1:g.16061A>T , LRG_250:g.16061A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000255078.8:c.800A>T MANE Select	ENSP00000255078.4:p.His267Leu
ENST00000539224.2:c.929A>T
ENST00000674955.1:c.800A>T	ENSP00000502463.1:p.His267Leu
ENST00000675118.1:c.147A>T
ENST00000675119.1:c.89A>T	ENSP00000501861.1:p.His30Leu
ENST00000675305.1:c.89A>T	ENSP00000502365.1:p.His30Leu
ENST00000675464.1:c.89A>T	ENSP00000502650.1:p.His30Leu
ENST00000675615.1:c.800A>T	ENSP00000502413.1:p.His267Leu
ENST00000675683.1:c.187A>T
ENST00000676173.1:n.844A>T
ENST00000676228.1:c.*123A>T	ENSP00000502375.1:n.*123A>T
ENST00000676239.1:n.114A>T
ENST00000255078.7:c.800A>T	ENSP00000255078.3:p.His267Leu
ENST00000539224.1:c.*123A>T	ENSP00000440465.1:n.*123A>T
NM_002180.2:c.800A>T , LRG_250t1:c.800A>T	NP_002171.2:p.His267Leu
XM_005273974.2:c.-212A>T	XP_005274031.1:n.-212A>T
XM_005273976.1:c.800A>T	XP_005274033.1:p.His267Leu
XR_247198.1:n.902A>T
XR_949903.1:n.902A>T
XM_005273976.2:c.800A>T	XP_005274033.1:p.His267Leu
XM_017017669.2:c.-212A>T	XP_016873158.1:n.-212A>T
XM_017017670.2:c.-212A>T	XP_016873159.1:n.-212A>T
XM_017017671.2:c.800A>T	XP_016873160.1:p.His267Leu
XR_949903.3:n.898A>T
NM_002180.3:c.800A>T MANE Select	NP_002171.2:p.His267Leu