Canonical Allele Identifier: CA2803979449

Gene: B2M

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.44711617_44711618insTTCAGGTTTACTCAC , CM000677.2:g.44711617_44711618insTTCAGGTTTACTCAC	GRCh38
NC_000015.9:g.45003815_45003816insTTCAGGTTTACTCAC , CM000677.1:g.45003815_45003816insTTCAGGTTTACTCAC	GRCh37
NC_000015.8:g.42791107_42791108insTTCAGGTTTACTCAC	NCBI36
NG_012920.1:g.5131_5132insTTCAGGTTTACTCAC
NG_012920.2:g.5141_5142insTTCAGGTTTACTCAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695792.1:n.83+177_83+178insTTCAGGTTTACTCAC
ENST00000648006.3:c.67+4_67+5insTTCAGGTTTACTCAC MANE Select	ENSP00000497910.1:n.67+4_67+5insTTCAGGTTTACTCAC
ENST00000349264.10:c.57+14_57+15insTTCAGGTTTACTCAC	ENSP00000340858.6:n.57+14_57+15insTTCAGGTTTACTCAC
ENST00000544417.5:c.67+4_67+5insTTCAGGTTTACTCAC	ENSP00000437604.2:n.67+4_67+5insTTCAGGTTTACTCAC
ENST00000557901.5:c.67+4_67+5insTTCAGGTTTACTCAC	ENSP00000452861.1:n.67+4_67+5insTTCAGGTTTACTCAC
ENST00000558401.5:c.67+4_67+5insTTCAGGTTTACTCAC	ENSP00000452780.1:n.67+4_67+5insTTCAGGTTTACTCAC
ENST00000559720.5:n.127+4_127+5insTTCAGGTTTACTCAC
ENST00000559916.1:c.67+4_67+5insTTCAGGTTTACTCAC	ENSP00000453350.1:n.67+4_67+5insTTCAGGTTTACTCAC
ENST00000561424.5:c.67+4_67+5insTTCAGGTTTACTCAC	ENSP00000453191.1:n.67+4_67+5insTTCAGGTTTACTCAC
NM_004048.2:c.67+4_67+5insTTCAGGTTTACTCAC	NP_004039.1:n.67+4_67+5insTTCAGGTTTACTCAC
XM_005254549.2:c.67+4_67+5insTTCAGGTTTACTCAC	XP_005254606.1:n.67+4_67+5insTTCAGGTTTACTCAC
NM_004048.3:c.67+4_67+5insTTCAGGTTTACTCAC	NP_004039.1:n.67+4_67+5insTTCAGGTTTACTCAC
XM_005254549.3:c.67+4_67+5insTTCAGGTTTACTCAC	XP_005254606.1:n.67+4_67+5insTTCAGGTTTACTCAC
XR_002957658.1:n.122+4_122+5insTTCAGGTTTACTCAC
NM_004048.4:c.67+4_67+5insTTCAGGTTTACTCAC MANE Select	NP_004039.1:n.67+4_67+5insTTCAGGTTTACTCAC