Canonical Allele Identifier: CA2173753474
Gene: B2M HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.44711752T= , CM000677.2:g.44711752T= GRCh38
NC_000015.9:g.45003950T= , CM000677.1:g.45003950T= GRCh37
NC_000015.8:g.42791242T= NCBI36
NG_012920.1:g.5266T=
NG_012920.2:g.5276T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000695792.1:n.83+312T=
ENST00000648006.3:c.67+139T= MANE Select ENSP00000497910.1:n.67+139T=
ENST00000349264.10:c.57+149T= ENSP00000340858.6:n.57+149T=
ENST00000544417.5:c.67+139T= ENSP00000437604.2:n.67+139T=
ENST00000557901.5:c.67+139T= ENSP00000452861.1:n.67+139T=
ENST00000558401.5:c.67+139T= ENSP00000452780.1:n.67+139T=
ENST00000559720.5:n.127+139T=
ENST00000559916.1:c.67+139T= ENSP00000453350.1:n.67+139T=
ENST00000561424.5:c.67+139T= ENSP00000453191.1:n.67+139T=
NM_004048.2:c.67+139T= NP_004039.1:n.67+139T=
XM_005254549.2:c.67+139T= XP_005254606.1:n.67+139T=
NM_004048.3:c.67+139T= NP_004039.1:n.67+139T=
XM_005254549.3:c.67+139T= XP_005254606.1:n.67+139T=
XR_002957658.1:n.122+139T=
NM_004048.4:c.67+139T= MANE Select NP_004039.1:n.67+139T=