Canonical Allele Identifier: CA2740093106

Gene: IGHMBP2

Linked Data

• ClinVar Variation Id: 2929307
• ClinVar RCV Id: RCV003782033

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68914814G>C , CM000673.2:g.68914814G>C	GRCh38
NC_000011.9:g.68682282G>C , CM000673.1:g.68682282G>C	GRCh37
NC_000011.8:g.68438858G>C	NCBI36
NG_007976.1:g.15964G>C , LRG_250:g.15964G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000255078.8:c.712-9G>C MANE Select	ENSP00000255078.4:n.712-9G>C
ENST00000539224.2:c.841-9G>C
ENST00000674955.1:c.712-9G>C	ENSP00000502463.1:n.712-9G>C
ENST00000675118.1:c.59-9G>C
ENST00000675615.1:c.712-9G>C	ENSP00000502413.1:n.712-9G>C
ENST00000675683.1:c.99-9G>C
ENST00000676173.1:n.756-9G>C
ENST00000676228.1:c.*35-9G>C	ENSP00000502375.1:n.*35-9G>C
ENST00000676239.1:n.26-9G>C
ENST00000255078.7:c.712-9G>C	ENSP00000255078.3:n.712-9G>C
ENST00000539224.1:c.*35-9G>C	ENSP00000440465.1:n.*35-9G>C
NM_002180.2:c.712-9G>C , LRG_250t1:c.712-9G>C	NP_002171.2:n.712-9G>C
XM_005273974.2:c.-300-9G>C	XP_005274031.1:n.-300-9G>C
XM_005273976.1:c.712-9G>C	XP_005274033.1:n.712-9G>C
XR_247198.1:n.814-9G>C
XR_949903.1:n.814-9G>C
XM_005273976.2:c.712-9G>C	XP_005274033.1:n.712-9G>C
XM_017017669.2:c.-300-9G>C	XP_016873158.1:n.-300-9G>C
XM_017017670.2:c.-300-9G>C	XP_016873159.1:n.-300-9G>C
XM_017017671.2:c.712-9G>C	XP_016873160.1:n.712-9G>C
XR_949903.3:n.810-9G>C
NM_002180.3:c.712-9G>C MANE Select	NP_002171.2:n.712-9G>C