Canonical Allele Identifier: CA2730861321

Gene: B2M

Linked Data

• dbSNP Id: rs2141284949

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.44711683_44711684del , CM000677.2:g.44711683_44711684del	GRCh38
NC_000015.9:g.45003881_45003882del , CM000677.1:g.45003881_45003882del	GRCh37
NC_000015.8:g.42791173_42791174del	NCBI36
NG_012920.1:g.5197_5198del
NG_012920.2:g.5207_5208del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695792.1:n.83+243_83+244del
ENST00000648006.3:c.67+70_67+71del MANE Select	ENSP00000497910.1:n.67+70_67+71del
ENST00000349264.10:c.57+80_57+81del	ENSP00000340858.6:n.57+80_57+81del
ENST00000544417.5:c.67+70_67+71del	ENSP00000437604.2:n.67+70_67+71del
ENST00000557901.5:c.67+70_67+71del	ENSP00000452861.1:n.67+70_67+71del
ENST00000558401.5:c.67+70_67+71del	ENSP00000452780.1:n.67+70_67+71del
ENST00000559720.5:n.127+70_127+71del
ENST00000559916.1:c.67+70_67+71del	ENSP00000453350.1:n.67+70_67+71del
ENST00000561424.5:c.67+70_67+71del	ENSP00000453191.1:n.67+70_67+71del
NM_004048.2:c.67+70_67+71del	NP_004039.1:n.67+70_67+71del
XM_005254549.2:c.67+70_67+71del	XP_005254606.1:n.67+70_67+71del
NM_004048.3:c.67+70_67+71del	NP_004039.1:n.67+70_67+71del
XM_005254549.3:c.67+70_67+71del	XP_005254606.1:n.67+70_67+71del
XR_002957658.1:n.122+70_122+71del
NM_004048.4:c.67+70_67+71del MANE Select	NP_004039.1:n.67+70_67+71del