Canonical Allele Identifier: CA381649804

Gene: IGHMBP2

Linked Data

• MyVariant Identifiers: chr11:g.68701297G>T (hg19) ; chr11:g.68933829G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68933829G>T , CM000673.2:g.68933829G>T	GRCh38
NC_000011.9:g.68701297G>T , CM000673.1:g.68701297G>T	GRCh37
NC_000011.8:g.68457873G>T	NCBI36
NG_007976.1:g.34979G>T , LRG_250:g.34979G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000255078.8:c.1453G>T MANE Select	ENSP00000255078.4:p.Gly485Cys
ENST00000674955.1:c.*170G>T	ENSP00000502463.1:n.*170G>T
ENST00000675118.1:c.941G>T
ENST00000675205.1:n.183+348G>T
ENST00000675615.1:c.1453G>T	ENSP00000502413.1:p.Gly485Cys
ENST00000675648.1:n.828G>T
ENST00000675997.1:n.113-635G>T
ENST00000676173.1:n.2198G>T
ENST00000676228.1:c.*776G>T	ENSP00000502375.1:n.*776G>T
ENST00000255078.7:c.1453G>T	ENSP00000255078.3:p.Gly485Cys
ENST00000537458.5:n.570G>T
ENST00000539064.5:n.1212G>T
ENST00000541229.5:n.148G>T
ENST00000543739.5:n.570G>T
NM_002180.2:c.1453G>T , LRG_250t1:c.1453G>T	NP_002171.2:p.Gly485Cys
XM_005273974.2:c.442G>T	XP_005274031.1:p.Gly148Cys
XM_005273975.2:c.325G>T	XP_005274032.1:p.Gly109Cys
XM_011544994.1:c.220G>T	XP_011543296.1:p.Gly74Cys
XR_949903.1:n.1555G>T
XM_005273975.3:c.325G>T	XP_005274032.1:p.Gly109Cys
XM_017017669.2:c.442G>T	XP_016873158.1:p.Gly148Cys
XM_017017670.2:c.442G>T	XP_016873159.1:p.Gly148Cys
XM_017017671.2:c.1453G>T	XP_016873160.1:p.Gly485Cys
XR_949903.3:n.1551G>T
NM_002180.3:c.1453G>T MANE Select	NP_002171.2:p.Gly485Cys