Canonical Allele Identifier: CA381653479

Gene: IGHMBP2

Linked Data

• gnomAD v4: 11-68936869-G-A
• MyVariant Identifiers: chr11:g.68704337G>A (hg19) ; chr11:g.68936869G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68936869G>A , CM000673.2:g.68936869G>A	GRCh38
NC_000011.9:g.68704337G>A , CM000673.1:g.68704337G>A	GRCh37
NC_000011.8:g.68460913G>A	NCBI36
NG_007976.1:g.38019G>A , LRG_250:g.38019G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000255078.8:c.2389G>A MANE Select	ENSP00000255078.4:p.Ala797Thr
ENST00000674675.1:c.587+46G>A
ENST00000674878.1:c.548-54G>A
ENST00000675118.1:c.1877G>A
ENST00000675389.1:n.664G>A
ENST00000675615.1:c.2389G>A	ENSP00000502413.1:p.Ala797Thr
ENST00000675648.1:n.1764G>A
ENST00000675916.1:c.633G>A
ENST00000676173.1:n.3134G>A
ENST00000676182.1:c.820G>A
ENST00000676228.1:c.*1712G>A	ENSP00000502375.1:n.*1712G>A
ENST00000255078.7:c.2389G>A	ENSP00000255078.3:p.Ala797Thr
ENST00000539064.5:n.2148G>A
ENST00000543739.5:n.1382G>A
NM_002180.2:c.2389G>A , LRG_250t1:c.2389G>A	NP_002171.2:p.Ala797Thr
XM_005273974.2:c.1378G>A	XP_005274031.1:p.Ala460Thr
XM_005273975.2:c.1261G>A	XP_005274032.1:p.Ala421Thr
XM_011544994.1:c.1156G>A	XP_011543296.1:p.Ala386Thr
XR_949903.1:n.2491G>A
XM_005273975.3:c.1261G>A	XP_005274032.1:p.Ala421Thr
XM_017017669.2:c.1378G>A	XP_016873158.1:p.Ala460Thr
XM_017017670.2:c.1378G>A	XP_016873159.1:p.Ala460Thr
XR_949903.3:n.2487G>A
NM_002180.3:c.2389G>A MANE Select	NP_002171.2:p.Ala797Thr