Canonical Allele Identifier: CA381653627

Gene: IGHMBP2

Linked Data

• gnomAD v4: 11-68936915-C-T
• MyVariant Identifiers: chr11:g.68704383C>T (hg19) ; chr11:g.68936915C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68936915C>T , CM000673.2:g.68936915C>T	GRCh38
NC_000011.9:g.68704383C>T , CM000673.1:g.68704383C>T	GRCh37
NC_000011.8:g.68460959C>T	NCBI36
NG_007976.1:g.38065C>T , LRG_250:g.38065C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000255078.8:c.2435C>T MANE Select	ENSP00000255078.4:p.Pro812Leu
ENST00000674675.1:c.588-8C>T
ENST00000674878.1:c.548-8C>T
ENST00000675118.1:c.1923C>T
ENST00000675389.1:n.710C>T
ENST00000675615.1:c.2435C>T	ENSP00000502413.1:p.Pro812Leu
ENST00000675648.1:n.1810C>T
ENST00000675916.1:c.679C>T
ENST00000676173.1:n.3180C>T
ENST00000676182.1:c.866C>T
ENST00000676228.1:c.*1758C>T	ENSP00000502375.1:n.*1758C>T
ENST00000255078.7:c.2435C>T	ENSP00000255078.3:p.Pro812Leu
ENST00000539064.5:n.2194C>T
ENST00000543739.5:n.1428C>T
NM_002180.2:c.2435C>T , LRG_250t1:c.2435C>T	NP_002171.2:p.Pro812Leu
XM_005273974.2:c.1424C>T	XP_005274031.1:p.Pro475Leu
XM_005273975.2:c.1307C>T	XP_005274032.1:p.Pro436Leu
XM_011544994.1:c.1202C>T	XP_011543296.1:p.Pro401Leu
XR_949903.1:n.2537C>T
XM_005273975.3:c.1307C>T	XP_005274032.1:p.Pro436Leu
XM_017017669.2:c.1424C>T	XP_016873158.1:p.Pro475Leu
XM_017017670.2:c.1424C>T	XP_016873159.1:p.Pro475Leu
XR_949903.3:n.2533C>T
NM_002180.3:c.2435C>T MANE Select	NP_002171.2:p.Pro812Leu