Canonical Allele Identifier: CA2614750413

Gene: IGHMBP2

Linked Data

• gnomAD v4: 11-68934183-A-ATTTTACGGCCTTCTC

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68934183_68934184insTTTTACGGCCTTCTC , CM000673.2:g.68934183_68934184insTTTTACGGCCTTCTC	GRCh38
NC_000011.9:g.68701651_68701652insTTTTACGGCCTTCTC , CM000673.1:g.68701651_68701652insTTTTACGGCCTTCTC	GRCh37
NC_000011.8:g.68458227_68458228insTTTTACGGCCTTCTC	NCBI36
NG_007976.1:g.35333_35334insTTTTACGGCCTTCTC , LRG_250:g.35333_35334insTTTTACGGCCTTCTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000255078.8:c.1537+270_1537+271insTTTTACGGCCTTCTC MANE Select	ENSP00000255078.4:n.1537+270_1537+271insTTTTACGGCCTTCTC
ENST00000674955.1:c.*254+270_*254+271insTTTTACGGCCTTCTC	ENSP00000502463.1:n.*254+270_*254+271insTTTTACGGCCTTCTC
ENST00000675118.1:c.1025+270_1025+271insTTTTACGGCCTTCTC
ENST00000675205.1:n.184-281_184-280insTTTTACGGCCTTCTC
ENST00000675615.1:c.1537+270_1537+271insTTTTACGGCCTTCTC	ENSP00000502413.1:n.1537+270_1537+271insTTTTACGGCCTTCTC
ENST00000675648.1:n.912+270_912+271insTTTTACGGCCTTCTC
ENST00000675997.1:n.113-281_113-280insTTTTACGGCCTTCTC
ENST00000676173.1:n.2282+270_2282+271insTTTTACGGCCTTCTC
ENST00000676228.1:c.*860+270_*860+271insTTTTACGGCCTTCTC	ENSP00000502375.1:n.*860+270_*860+271insTTTTACGGCCTTCTC
ENST00000255078.7:c.1537+270_1537+271insTTTTACGGCCTTCTC	ENSP00000255078.3:n.1537+270_1537+271insTTTTACGGCCTTCTC
ENST00000539064.5:n.1296+270_1296+271insTTTTACGGCCTTCTC
ENST00000541229.5:n.232+270_232+271insTTTTACGGCCTTCTC
ENST00000543739.5:n.654+270_654+271insTTTTACGGCCTTCTC
NM_002180.2:c.1537+270_1537+271insTTTTACGGCCTTCTC , LRG_250t1:c.1537+270_1537+271insTTTTACGGCCTTCTC	NP_002171.2:n.1537+270_1537+271insTTTTACGGCCTTCTC
XM_005273974.2:c.526+270_526+271insTTTTACGGCCTTCTC	XP_005274031.1:n.526+270_526+271insTTTTACGGCCTTCTC
XM_005273975.2:c.409+270_409+271insTTTTACGGCCTTCTC	XP_005274032.1:n.409+270_409+271insTTTTACGGCCTTCTC
XM_011544994.1:c.304+270_304+271insTTTTACGGCCTTCTC	XP_011543296.1:n.304+270_304+271insTTTTACGGCCTTCTC
XR_949903.1:n.1639+270_1639+271insTTTTACGGCCTTCTC
XM_005273975.3:c.409+270_409+271insTTTTACGGCCTTCTC	XP_005274032.1:n.409+270_409+271insTTTTACGGCCTTCTC
XM_017017669.2:c.526+270_526+271insTTTTACGGCCTTCTC	XP_016873158.1:n.526+270_526+271insTTTTACGGCCTTCTC
XM_017017670.2:c.526+270_526+271insTTTTACGGCCTTCTC	XP_016873159.1:n.526+270_526+271insTTTTACGGCCTTCTC
XM_017017671.2:c.1537+270_1537+271insTTTTACGGCCTTCTC	XP_016873160.1:n.1537+270_1537+271insTTTTACGGCCTTCTC
XR_949903.3:n.1635+270_1635+271insTTTTACGGCCTTCTC
NM_002180.3:c.1537+270_1537+271insTTTTACGGCCTTCTC MANE Select	NP_002171.2:n.1537+270_1537+271insTTTTACGGCCTTCTC