Canonical Allele Identifier: CA2730859696

Gene: B2M

Linked Data

• dbSNP Id: rs2141284518

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.44711579_44711580del , CM000677.2:g.44711579_44711580del	GRCh38
NC_000015.9:g.45003777_45003778del , CM000677.1:g.45003777_45003778del	GRCh37
NC_000015.8:g.42791069_42791070del	NCBI36
NG_012920.1:g.5093_5094del
NG_012920.2:g.5103_5104del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695792.1:n.83+139_83+140del
ENST00000648006.3:c.33_34del MANE Select	ENSP00000497910.1:p.Leu12ThrfsTer?
ENST00000349264.10:c.33_34del	ENSP00000340858.6:p.Leu12ThrfsTer?
ENST00000544417.5:c.33_34del	ENSP00000437604.2:p.Leu12ThrfsTer26
ENST00000557901.5:c.33_34del	ENSP00000452861.1:p.Leu12ThrfsTer28
ENST00000558401.5:c.33_34del	ENSP00000452780.1:p.Leu12ThrfsTer?
ENST00000559720.5:n.93_94del
ENST00000559916.1:c.33_34del	ENSP00000453350.1:p.Leu12ThrfsTer?
ENST00000561424.5:c.33_34del	ENSP00000453191.1:p.Leu12ThrfsTer?
NM_004048.2:c.33_34del	NP_004039.1:p.Leu12ThrfsTer?
XM_005254549.2:c.33_34del	XP_005254606.1:p.Leu12ThrfsTer?
NM_004048.3:c.33_34del	NP_004039.1:p.Leu12ThrfsTer?
XM_005254549.3:c.33_34del	XP_005254606.1:p.Leu12ThrfsTer?
XR_002957658.1:n.88_89del
NM_004048.4:c.33_34del MANE Select	NP_004039.1:p.Leu12ThrfsTer?