Canonical Allele Identifier: CA381650009

Gene: IGHMBP2

Linked Data

• dbSNP Id: rs201964221
• gnomAD v2: 11-68701327-G-C
• gnomAD v4: 11-68933859-G-C
• MyVariant Identifiers: chr11:g.68701327G>C (hg19) ; chr11:g.68933859G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68933859G>C , CM000673.2:g.68933859G>C	GRCh38
NC_000011.9:g.68701327G>C , CM000673.1:g.68701327G>C	GRCh37
NC_000011.8:g.68457903G>C	NCBI36
NG_007976.1:g.35009G>C , LRG_250:g.35009G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000255078.8:c.1483G>C MANE Select	ENSP00000255078.4:p.Gly495Arg
ENST00000674955.1:c.*200G>C	ENSP00000502463.1:n.*200G>C
ENST00000675118.1:c.971G>C
ENST00000675205.1:n.183+378G>C
ENST00000675615.1:c.1483G>C	ENSP00000502413.1:p.Gly495Arg
ENST00000675648.1:n.858G>C
ENST00000675997.1:n.113-605G>C
ENST00000676173.1:n.2228G>C
ENST00000676228.1:c.*806G>C	ENSP00000502375.1:n.*806G>C
ENST00000255078.7:c.1483G>C	ENSP00000255078.3:p.Gly495Arg
ENST00000537458.5:n.600G>C
ENST00000539064.5:n.1242G>C
ENST00000541229.5:n.178G>C
ENST00000543739.5:n.600G>C
NM_002180.2:c.1483G>C , LRG_250t1:c.1483G>C	NP_002171.2:p.Gly495Arg
XM_005273974.2:c.472G>C	XP_005274031.1:p.Gly158Arg
XM_005273975.2:c.355G>C	XP_005274032.1:p.Gly119Arg
XM_011544994.1:c.250G>C	XP_011543296.1:p.Gly84Arg
XR_949903.1:n.1585G>C
XM_005273975.3:c.355G>C	XP_005274032.1:p.Gly119Arg
XM_017017669.2:c.472G>C	XP_016873158.1:p.Gly158Arg
XM_017017670.2:c.472G>C	XP_016873159.1:p.Gly158Arg
XM_017017671.2:c.1483G>C	XP_016873160.1:p.Gly495Arg
XR_949903.3:n.1581G>C
NM_002180.3:c.1483G>C MANE Select	NP_002171.2:p.Gly495Arg