Canonical Allele Identifier: CA679620084

Gene: IGHMBP2

Linked Data

• dbSNP Id: rs1378656193
• gnomAD v3: 11-68908006-T-TA
• gnomAD v4: 11-68908006-T-TA
• MyVariant Identifiers: chr11:g.68675474_68675475insA (hg19) ; chr11:g.68908006_68908007insA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68908006_68908007insA , CM000673.2:g.68908006_68908007insA	GRCh38
NC_000011.9:g.68675474_68675475insA , CM000673.1:g.68675474_68675475insA	GRCh37
NC_000011.8:g.68432050_68432051insA	NCBI36
NG_007976.1:g.9156_9157insA , LRG_250:g.9156_9157insA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000255078.8:c.257-139_257-138insA MANE Select	ENSP00000255078.4:n.257-139_257-138insA
ENST00000539224.2:c.220-139_220-138insA
ENST00000674583.1:c.220-139_220-138insA
ENST00000674597.1:c.68-139_68-138insA
ENST00000674955.1:c.257-139_257-138insA	ENSP00000502463.1:n.257-139_257-138insA
ENST00000675142.1:n.220-139_220-138insA
ENST00000675469.1:c.133-139_133-138insA
ENST00000675615.1:c.257-139_257-138insA	ENSP00000502413.1:n.257-139_257-138insA
ENST00000675674.1:n.220-139_220-138insA
ENST00000675873.1:c.220-139_220-138insA
ENST00000676173.1:n.301-139_301-138insA
ENST00000676228.1:c.257-139_257-138insA	ENSP00000502375.1:n.257-139_257-138insA
ENST00000255078.7:c.257-139_257-138insA	ENSP00000255078.3:n.257-139_257-138insA
ENST00000539224.1:c.257-139_257-138insA	ENSP00000440465.1:n.257-139_257-138insA
ENST00000544541.1:c.87-139_87-138insA	ENSP00000443343.1:n.87-139_87-138insA
ENST00000545146.1:c.*127-139_*127-138insA	ENSP00000456366.1:n.*127-139_*127-138insA
NM_002180.2:c.257-139_257-138insA , LRG_250t1:c.257-139_257-138insA	NP_002171.2:n.257-139_257-138insA
XM_005273974.2:c.-755-139_-755-138insA	XP_005274031.1:n.-755-139_-755-138insA
XM_005273976.1:c.257-139_257-138insA	XP_005274033.1:n.257-139_257-138insA
XR_247198.1:n.359-139_359-138insA
XR_949903.1:n.359-139_359-138insA
XM_005273976.2:c.257-139_257-138insA	XP_005274033.1:n.257-139_257-138insA
XM_017017669.2:c.-657-139_-657-138insA	XP_016873158.1:n.-657-139_-657-138insA
XM_017017671.2:c.257-139_257-138insA	XP_016873160.1:n.257-139_257-138insA
XR_949903.3:n.355-139_355-138insA
NM_002180.3:c.257-139_257-138insA MANE Select	NP_002171.2:n.257-139_257-138insA