Canonical Allele Identifier: CA645576713
Gene: B2M HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.44711567_44711577del , CM000677.2:g.44711567_44711577del GRCh38
NC_000015.9:g.45003765_45003775del , CM000677.1:g.45003765_45003775del GRCh37
NC_000015.8:g.42791057_42791067del NCBI36
NG_012920.1:g.5081_5091del
NG_012920.2:g.5091_5101del

Transcript Alleles

HGVS Amino-acid Change
ENST00000695792.1:n.83+127_83+137del
ENST00000648006.3:c.21_31del MANE Select ENSP00000497910.1:p.Leu7PhefsTer?
ENST00000349264.10:c.21_31del ENSP00000340858.6:p.Leu7PhefsTer?
ENST00000544417.5:c.21_31del ENSP00000437604.2:p.Leu7PhefsTer28
ENST00000557901.5:c.21_31del ENSP00000452861.1:p.Leu7PhefsTer30
ENST00000558401.5:c.21_31del ENSP00000452780.1:p.Leu7PhefsTer?
ENST00000559720.5:n.81_91del
ENST00000559916.1:c.21_31del ENSP00000453350.1:p.Leu7PhefsTer?
ENST00000561424.5:c.21_31del ENSP00000453191.1:p.Leu7PhefsTer?
NM_004048.2:c.21_31del NP_004039.1:p.Leu7PhefsTer?
XM_005254549.2:c.21_31del XP_005254606.1:p.Leu7PhefsTer?
NM_004048.3:c.21_31del NP_004039.1:p.Leu7PhefsTer?
XM_005254549.3:c.21_31del XP_005254606.1:p.Leu7PhefsTer?
XR_002957658.1:n.76_86del
NM_004048.4:c.21_31del MANE Select NP_004039.1:p.Leu7PhefsTer?