Canonical Allele Identifier: CA2173753342
Gene: B2M HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.44711512C= , CM000677.2:g.44711512C= GRCh38
NC_000015.9:g.45003710C= , CM000677.1:g.45003710C= GRCh37
NC_000015.8:g.42791002C= NCBI36
NG_012920.1:g.5026C=
NG_012920.2:g.5036C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000695792.1:n.83+72C=
ENST00000544417.5:c.-35C= ENSP00000437604.2:n.-35C=
ENST00000558401.5:c.-35C= ENSP00000452780.1:n.-35C=
ENST00000559720.5:n.26C=
ENST00000561424.5:c.-35C= ENSP00000453191.1:n.-35C=
NM_004048.2:c.-35C= NP_004039.1:n.-35C=
XM_005254549.2:c.-35C= XP_005254606.1:n.-35C=
XM_005254549.3:c.-35C= XP_005254606.1:n.-35C=
XR_002957658.1:n.21C=