Canonical Allele Identifier: CA381654009

Gene: IGHMBP2

Linked Data

• gnomAD v4: 11-68937046-T-A
• MyVariant Identifiers: chr11:g.68704514T>A (hg19) ; chr11:g.68937046T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68937046T>A , CM000673.2:g.68937046T>A	GRCh38
NC_000011.9:g.68704514T>A , CM000673.1:g.68704514T>A	GRCh37
NC_000011.8:g.68461090T>A	NCBI36
NG_007976.1:g.38196T>A , LRG_250:g.38196T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000255078.8:c.2566T>A MANE Select	ENSP00000255078.4:p.Ser856Thr
ENST00000674675.1:c.711T>A
ENST00000674878.1:c.671T>A
ENST00000675118.1:c.2054T>A
ENST00000675389.1:n.841T>A
ENST00000675615.1:c.2566T>A	ENSP00000502413.1:p.Ser856Thr
ENST00000675648.1:n.1941T>A
ENST00000675916.1:c.810T>A
ENST00000676173.1:n.3311T>A
ENST00000676182.1:c.997T>A
ENST00000676228.1:c.*1889T>A	ENSP00000502375.1:n.*1889T>A
ENST00000255078.7:c.2566T>A	ENSP00000255078.3:p.Ser856Thr
ENST00000539064.5:n.2325T>A
ENST00000543739.5:n.1559T>A
NM_002180.2:c.2566T>A , LRG_250t1:c.2566T>A	NP_002171.2:p.Ser856Thr
XM_005273974.2:c.1555T>A	XP_005274031.1:p.Ser519Thr
XM_005273975.2:c.1438T>A	XP_005274032.1:p.Ser480Thr
XM_011544994.1:c.1333T>A	XP_011543296.1:p.Ser445Thr
XR_949903.1:n.2668T>A
XM_005273975.3:c.1438T>A	XP_005274032.1:p.Ser480Thr
XM_017017669.2:c.1555T>A	XP_016873158.1:p.Ser519Thr
XM_017017670.2:c.1555T>A	XP_016873159.1:p.Ser519Thr
XR_949903.3:n.2664T>A
NM_002180.3:c.2566T>A MANE Select	NP_002171.2:p.Ser856Thr