Canonical Allele Identifier: CA223392659

Gene: IGHMBP2

Linked Data

• ClinVar Variation Id: 2937972
• ClinVar RCV Id: RCV003796794
• dbSNP Id: rs373767876
• MyVariant Identifiers: chr11:g.68682502T>C (hg19) ; chr11:g.68915034T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68915034T>C , CM000673.2:g.68915034T>C	GRCh38
NC_000011.9:g.68682502T>C , CM000673.1:g.68682502T>C	GRCh37
NC_000011.8:g.68439078T>C	NCBI36
NG_007976.1:g.16184T>C , LRG_250:g.16184T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000255078.8:c.912+11T>C MANE Select	ENSP00000255078.4:n.912+11T>C
ENST00000539224.2:c.1041+11T>C
ENST00000674955.1:c.912+11T>C	ENSP00000502463.1:n.912+11T>C
ENST00000675118.1:c.259+11T>C
ENST00000675119.1:c.201+11T>C	ENSP00000501861.1:n.201+11T>C
ENST00000675305.1:c.201+11T>C	ENSP00000502365.1:n.201+11T>C
ENST00000675464.1:c.195+17T>C	ENSP00000502650.1:n.195+17T>C
ENST00000675615.1:c.912+11T>C	ENSP00000502413.1:n.912+11T>C
ENST00000675683.1:c.299+11T>C
ENST00000676173.1:n.956+11T>C
ENST00000676228.1:c.*235+11T>C	ENSP00000502375.1:n.*235+11T>C
ENST00000255078.7:c.912+11T>C	ENSP00000255078.3:n.912+11T>C
NM_002180.2:c.912+11T>C , LRG_250t1:c.912+11T>C	NP_002171.2:n.912+11T>C
XM_005273974.2:c.-100+11T>C	XP_005274031.1:n.-100+11T>C
XM_005273976.1:c.912+11T>C	XP_005274033.1:n.912+11T>C
XR_247198.1:n.1014+11T>C
XR_949903.1:n.1014+11T>C
XM_005273976.2:c.912+11T>C	XP_005274033.1:n.912+11T>C
XM_017017669.2:c.-100+11T>C	XP_016873158.1:n.-100+11T>C
XM_017017670.2:c.-100+11T>C	XP_016873159.1:n.-100+11T>C
XM_017017671.2:c.912+11T>C	XP_016873160.1:n.912+11T>C
XR_949903.3:n.1010+11T>C
NM_002180.3:c.912+11T>C MANE Select	NP_002171.2:n.912+11T>C