Canonical Allele Identifier: CA2173753475

Gene: B2M

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.44711759_44711760delinsCG , CM000677.2:g.44711759_44711760delinsCG	GRCh38
NC_000015.9:g.45003957_45003958delinsCG , CM000677.1:g.45003957_45003958delinsCG	GRCh37
NC_000015.8:g.42791249_42791250delinsCG	NCBI36
NG_012920.1:g.5273_5274delinsCG
NG_012920.2:g.5283_5284delinsCG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695792.1:n.83+319_83+320delinsCG
ENST00000648006.3:c.67+146_67+147delinsCG MANE Select	ENSP00000497910.1:n.67+146_67+147delinsCG
ENST00000349264.10:c.57+156_57+157delinsCG	ENSP00000340858.6:n.57+156_57+157delinsCG
ENST00000544417.5:c.67+146_67+147delinsCG	ENSP00000437604.2:n.67+146_67+147delinsCG
ENST00000557901.5:c.67+146_67+147delinsCG	ENSP00000452861.1:n.67+146_67+147delinsCG
ENST00000558401.5:c.67+146_67+147delinsCG	ENSP00000452780.1:n.67+146_67+147delinsCG
ENST00000559720.5:n.127+146_127+147delinsCG
ENST00000559916.1:c.67+146_67+147delinsCG	ENSP00000453350.1:n.67+146_67+147delinsCG
ENST00000561424.5:c.67+146_67+147delinsCG	ENSP00000453191.1:n.67+146_67+147delinsCG
NM_004048.2:c.67+146_67+147delinsCG	NP_004039.1:n.67+146_67+147delinsCG
XM_005254549.2:c.67+146_67+147delinsCG	XP_005254606.1:n.67+146_67+147delinsCG
NM_004048.3:c.67+146_67+147delinsCG	NP_004039.1:n.67+146_67+147delinsCG
XM_005254549.3:c.67+146_67+147delinsCG	XP_005254606.1:n.67+146_67+147delinsCG
XR_002957658.1:n.122+146_122+147delinsCG
NM_004048.4:c.67+146_67+147delinsCG MANE Select	NP_004039.1:n.67+146_67+147delinsCG