Canonical Allele Identifier: CA645576716
Gene: B2M HGNC NCBI

Linked Data

COSMIC: COSM144578

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.44711577_44711587del , CM000677.2:g.44711577_44711587del GRCh38
NC_000015.9:g.45003775_45003785del , CM000677.1:g.45003775_45003785del GRCh37
NC_000015.8:g.42791067_42791077del NCBI36
NG_012920.1:g.5091_5101del
NG_012920.2:g.5101_5111del

Transcript Alleles

HGVS Amino-acid Change
ENST00000695792.1:n.83+137_83+147del
ENST00000648006.3:c.31_41del MANE Select ENSP00000497910.1:p.Ala11SerfsTer?
ENST00000349264.10:c.31_41del ENSP00000340858.6:p.Ala11SerfsTer?
ENST00000544417.5:c.31_41del ENSP00000437604.2:p.Ala11SerfsTer24
ENST00000557901.5:c.31_41del ENSP00000452861.1:p.Ala11SerfsTer26
ENST00000558401.5:c.31_41del ENSP00000452780.1:p.Ala11SerfsTer?
ENST00000559720.5:n.91_101del
ENST00000559916.1:c.31_41del ENSP00000453350.1:p.Ala11SerfsTer?
ENST00000561424.5:c.31_41del ENSP00000453191.1:p.Ala11SerfsTer?
NM_004048.2:c.31_41del NP_004039.1:p.Ala11SerfsTer?
XM_005254549.2:c.31_41del XP_005254606.1:p.Ala11SerfsTer?
NM_004048.3:c.31_41del NP_004039.1:p.Ala11SerfsTer?
XM_005254549.3:c.31_41del XP_005254606.1:p.Ala11SerfsTer?
XR_002957658.1:n.86_96del
NM_004048.4:c.31_41del MANE Select NP_004039.1:p.Ala11SerfsTer?