Canonical Allele Identifier: CA381653905

Gene: IGHMBP2

Linked Data

• gnomAD v4: 11-68937017-G-T
• MyVariant Identifiers: chr11:g.68704485G>T (hg19) ; chr11:g.68937017G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68937017G>T , CM000673.2:g.68937017G>T	GRCh38
NC_000011.9:g.68704485G>T , CM000673.1:g.68704485G>T	GRCh37
NC_000011.8:g.68461061G>T	NCBI36
NG_007976.1:g.38167G>T , LRG_250:g.38167G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000255078.8:c.2537G>T MANE Select	ENSP00000255078.4:p.Gly846Val
ENST00000674675.1:c.682G>T
ENST00000674878.1:c.642G>T
ENST00000675118.1:c.2025G>T
ENST00000675389.1:n.812G>T
ENST00000675615.1:c.2537G>T	ENSP00000502413.1:p.Gly846Val
ENST00000675648.1:n.1912G>T
ENST00000675916.1:c.781G>T
ENST00000676173.1:n.3282G>T
ENST00000676182.1:c.968G>T
ENST00000676228.1:c.*1860G>T	ENSP00000502375.1:n.*1860G>T
ENST00000255078.7:c.2537G>T	ENSP00000255078.3:p.Gly846Val
ENST00000539064.5:n.2296G>T
ENST00000543739.5:n.1530G>T
NM_002180.2:c.2537G>T , LRG_250t1:c.2537G>T	NP_002171.2:p.Gly846Val
XM_005273974.2:c.1526G>T	XP_005274031.1:p.Gly509Val
XM_005273975.2:c.1409G>T	XP_005274032.1:p.Gly470Val
XM_011544994.1:c.1304G>T	XP_011543296.1:p.Gly435Val
XR_949903.1:n.2639G>T
XM_005273975.3:c.1409G>T	XP_005274032.1:p.Gly470Val
XM_017017669.2:c.1526G>T	XP_016873158.1:p.Gly509Val
XM_017017670.2:c.1526G>T	XP_016873159.1:p.Gly509Val
XR_949903.3:n.2635G>T
NM_002180.3:c.2537G>T MANE Select	NP_002171.2:p.Gly846Val