Canonical Allele Identifier: CA2614749377

Gene: IGHMBP2

Linked Data

• gnomAD v4: 11-68933641-G-GCCTGACCCAGCTCTCCA

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68933641_68933642insCCTGACCCAGCTCTCCA , CM000673.2:g.68933641_68933642insCCTGACCCAGCTCTCCA	GRCh38
NC_000011.9:g.68701109_68701110insCCTGACCCAGCTCTCCA , CM000673.1:g.68701109_68701110insCCTGACCCAGCTCTCCA	GRCh37
NC_000011.8:g.68457685_68457686insCCTGACCCAGCTCTCCA	NCBI36
NG_007976.1:g.34791_34792insCCTGACCCAGCTCTCCA , LRG_250:g.34791_34792insCCTGACCCAGCTCTCCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000255078.8:c.1419-154_1419-153insCCTGACCCAGCTCTCCA MANE Select	ENSP00000255078.4:n.1419-154_1419-153insCCTGACCCAGCTCTCCA
ENST00000674955.1:c.*136-154_*136-153insCCTGACCCAGCTCTCCA	ENSP00000502463.1:n.*136-154_*136-153insCCTGACCCAGCTCTCCA
ENST00000675118.1:c.907-154_907-153insCCTGACCCAGCTCTCCA
ENST00000675205.1:n.183+160_183+161insCCTGACCCAGCTCTCCA
ENST00000675615.1:c.1419-154_1419-153insCCTGACCCAGCTCTCCA	ENSP00000502413.1:n.1419-154_1419-153insCCTGACCCAGCTCTCCA
ENST00000675648.1:n.794-154_794-153insCCTGACCCAGCTCTCCA
ENST00000675997.1:n.113-823_113-822insCCTGACCCAGCTCTCCA
ENST00000676173.1:n.2164-154_2164-153insCCTGACCCAGCTCTCCA
ENST00000676228.1:c.*742-154_*742-153insCCTGACCCAGCTCTCCA	ENSP00000502375.1:n.*742-154_*742-153insCCTGACCCAGCTCTCCA
ENST00000255078.7:c.1419-154_1419-153insCCTGACCCAGCTCTCCA	ENSP00000255078.3:n.1419-154_1419-153insCCTGACCCAGCTCTCCA
ENST00000537458.5:n.536-154_536-153insCCTGACCCAGCTCTCCA
ENST00000539064.5:n.1178-154_1178-153insCCTGACCCAGCTCTCCA
ENST00000543739.5:n.536-154_536-153insCCTGACCCAGCTCTCCA
NM_002180.2:c.1419-154_1419-153insCCTGACCCAGCTCTCCA , LRG_250t1:c.1419-154_1419-153insCCTGACCCAGCTCTCCA	NP_002171.2:n.1419-154_1419-153insCCTGACCCAGCTCTCCA
XM_005273974.2:c.408-154_408-153insCCTGACCCAGCTCTCCA	XP_005274031.1:n.408-154_408-153insCCTGACCCAGCTCTCCA
XM_005273975.2:c.291-154_291-153insCCTGACCCAGCTCTCCA	XP_005274032.1:n.291-154_291-153insCCTGACCCAGCTCTCCA
XM_011544994.1:c.186-154_186-153insCCTGACCCAGCTCTCCA	XP_011543296.1:n.186-154_186-153insCCTGACCCAGCTCTCCA
XR_949903.1:n.1521-154_1521-153insCCTGACCCAGCTCTCCA
XM_005273975.3:c.291-154_291-153insCCTGACCCAGCTCTCCA	XP_005274032.1:n.291-154_291-153insCCTGACCCAGCTCTCCA
XM_017017669.2:c.408-154_408-153insCCTGACCCAGCTCTCCA	XP_016873158.1:n.408-154_408-153insCCTGACCCAGCTCTCCA
XM_017017670.2:c.408-154_408-153insCCTGACCCAGCTCTCCA	XP_016873159.1:n.408-154_408-153insCCTGACCCAGCTCTCCA
XM_017017671.2:c.1419-154_1419-153insCCTGACCCAGCTCTCCA	XP_016873160.1:n.1419-154_1419-153insCCTGACCCAGCTCTCCA
XR_949903.3:n.1517-154_1517-153insCCTGACCCAGCTCTCCA
NM_002180.3:c.1419-154_1419-153insCCTGACCCAGCTCTCCA MANE Select	NP_002171.2:n.1419-154_1419-153insCCTGACCCAGCTCTCCA