Canonical Allele Identifier: CA2730860544

Gene: B2M

Linked Data

• dbSNP Id: rs2141284715

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.44711617_44711618insTTCAGGTTTACTCACGTCATCCAGCAGAGAATGGAAA , CM000677.2:g.44711617_44711618insTTCAGGTTTACTCACGTCATCCAGCAGAGAATGGAAA	GRCh38
NC_000015.9:g.45003815_45003816insTTCAGGTTTACTCACGTCATCCAGCAGAGAATGGAAA , CM000677.1:g.45003815_45003816insTTCAGGTTTACTCACGTCATCCAGCAGAGAATGGAAA	GRCh37
NC_000015.8:g.42791107_42791108insTTCAGGTTTACTCACGTCATCCAGCAGAGAATGGAAA	NCBI36
NG_012920.1:g.5131_5132insTTCAGGTTTACTCACGTCATCCAGCAGAGAATGGAAA
NG_012920.2:g.5141_5142insTTCAGGTTTACTCACGTCATCCAGCAGAGAATGGAAA

Transcript Alleles

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