Canonical Allele Identifier: CA381650283

Gene: IGHMBP2

Linked Data

• MyVariant Identifiers: chr11:g.68701365G>T (hg19) ; chr11:g.68933897G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68933897G>T , CM000673.2:g.68933897G>T	GRCh38
NC_000011.9:g.68701365G>T , CM000673.1:g.68701365G>T	GRCh37
NC_000011.8:g.68457941G>T	NCBI36
NG_007976.1:g.35047G>T , LRG_250:g.35047G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000255078.8:c.1521G>T MANE Select	ENSP00000255078.4:p.Gln507His
ENST00000674955.1:c.*238G>T	ENSP00000502463.1:n.*238G>T
ENST00000675118.1:c.1009G>T
ENST00000675205.1:n.183+416G>T
ENST00000675615.1:c.1521G>T	ENSP00000502413.1:p.Gln507His
ENST00000675648.1:n.896G>T
ENST00000675997.1:n.113-567G>T
ENST00000676173.1:n.2266G>T
ENST00000676228.1:c.*844G>T	ENSP00000502375.1:n.*844G>T
ENST00000255078.7:c.1521G>T	ENSP00000255078.3:p.Gln507His
ENST00000537458.5:n.638G>T
ENST00000539064.5:n.1280G>T
ENST00000541229.5:n.216G>T
ENST00000543739.5:n.638G>T
NM_002180.2:c.1521G>T , LRG_250t1:c.1521G>T	NP_002171.2:p.Gln507His
XM_005273974.2:c.510G>T	XP_005274031.1:p.Gln170His
XM_005273975.2:c.393G>T	XP_005274032.1:p.Gln131His
XM_011544994.1:c.288G>T	XP_011543296.1:p.Gln96His
XR_949903.1:n.1623G>T
XM_005273975.3:c.393G>T	XP_005274032.1:p.Gln131His
XM_017017669.2:c.510G>T	XP_016873158.1:p.Gln170His
XM_017017670.2:c.510G>T	XP_016873159.1:p.Gln170His
XM_017017671.2:c.1521G>T	XP_016873160.1:p.Gln507His
XR_949903.3:n.1619G>T
NM_002180.3:c.1521G>T MANE Select	NP_002171.2:p.Gln507His