Canonical Allele Identifier: CA645576717
Gene: B2M HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.44711589_44711590del , CM000677.2:g.44711589_44711590del GRCh38
NC_000015.9:g.45003787_45003788del , CM000677.1:g.45003787_45003788del GRCh37
NC_000015.8:g.42791079_42791080del NCBI36
NG_012920.1:g.5103_5104del
NG_012920.2:g.5113_5114del

Transcript Alleles

HGVS Amino-acid Change
ENST00000695792.1:n.83+149_83+150del
ENST00000648006.3:c.43_44del MANE Select ENSP00000497910.1:p.Leu15PhefsTer?
ENST00000349264.10:c.43_44del ENSP00000340858.6:p.Leu15PhefsTer?
ENST00000544417.5:c.43_44del ENSP00000437604.2:p.Leu15PhefsTer23
ENST00000557901.5:c.43_44del ENSP00000452861.1:p.Leu15PhefsTer25
ENST00000558401.5:c.43_44del ENSP00000452780.1:p.Leu15PhefsTer?
ENST00000559720.5:n.103_104del
ENST00000559916.1:c.43_44del ENSP00000453350.1:p.Leu15PhefsTer?
ENST00000561424.5:c.43_44del ENSP00000453191.1:p.Leu15PhefsTer?
NM_004048.2:c.43_44del NP_004039.1:p.Leu15PhefsTer?
XM_005254549.2:c.43_44del XP_005254606.1:p.Leu15PhefsTer?
NM_004048.3:c.43_44del NP_004039.1:p.Leu15PhefsTer?
XM_005254549.3:c.43_44del XP_005254606.1:p.Leu15PhefsTer?
XR_002957658.1:n.98_99del
NM_004048.4:c.43_44del MANE Select NP_004039.1:p.Leu15PhefsTer?