Canonical Allele Identifier: CA381653499

Gene: IGHMBP2

Linked Data

• gnomAD v4: 11-68936876-C-A
• MyVariant Identifiers: chr11:g.68704344C>A (hg19) ; chr11:g.68936876C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68936876C>A , CM000673.2:g.68936876C>A	GRCh38
NC_000011.9:g.68704344C>A , CM000673.1:g.68704344C>A	GRCh37
NC_000011.8:g.68460920C>A	NCBI36
NG_007976.1:g.38026C>A , LRG_250:g.38026C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000255078.8:c.2396C>A MANE Select	ENSP00000255078.4:p.Thr799Asn
ENST00000674675.1:c.588-47C>A
ENST00000674878.1:c.548-47C>A
ENST00000675118.1:c.1884C>A
ENST00000675389.1:n.671C>A
ENST00000675615.1:c.2396C>A	ENSP00000502413.1:p.Thr799Asn
ENST00000675648.1:n.1771C>A
ENST00000675916.1:c.640C>A
ENST00000676173.1:n.3141C>A
ENST00000676182.1:c.827C>A
ENST00000676228.1:c.*1719C>A	ENSP00000502375.1:n.*1719C>A
ENST00000255078.7:c.2396C>A	ENSP00000255078.3:p.Thr799Asn
ENST00000539064.5:n.2155C>A
ENST00000543739.5:n.1389C>A
NM_002180.2:c.2396C>A , LRG_250t1:c.2396C>A	NP_002171.2:p.Thr799Asn
XM_005273974.2:c.1385C>A	XP_005274031.1:p.Thr462Asn
XM_005273975.2:c.1268C>A	XP_005274032.1:p.Thr423Asn
XM_011544994.1:c.1163C>A	XP_011543296.1:p.Thr388Asn
XR_949903.1:n.2498C>A
XM_005273975.3:c.1268C>A	XP_005274032.1:p.Thr423Asn
XM_017017669.2:c.1385C>A	XP_016873158.1:p.Thr462Asn
XM_017017670.2:c.1385C>A	XP_016873159.1:p.Thr462Asn
XR_949903.3:n.2494C>A
NM_002180.3:c.2396C>A MANE Select	NP_002171.2:p.Thr799Asn