Canonical Allele Identifier: CA2173753438

Gene: B2M

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.44711652C= , CM000677.2:g.44711652C=	GRCh38
NC_000015.9:g.45003850C= , CM000677.1:g.45003850C=	GRCh37
NC_000015.8:g.42791142C=	NCBI36
NG_012920.1:g.5166C=
NG_012920.2:g.5176C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695792.1:n.83+212C=
ENST00000648006.3:c.67+39C= MANE Select	ENSP00000497910.1:n.67+39C=
ENST00000349264.10:c.57+49C=	ENSP00000340858.6:n.57+49C=
ENST00000544417.5:c.67+39C=	ENSP00000437604.2:n.67+39C=
ENST00000557901.5:c.67+39C=	ENSP00000452861.1:n.67+39C=
ENST00000558401.5:c.67+39C=	ENSP00000452780.1:n.67+39C=
ENST00000559720.5:n.127+39C=
ENST00000559916.1:c.67+39C=	ENSP00000453350.1:n.67+39C=
ENST00000561424.5:c.67+39C=	ENSP00000453191.1:n.67+39C=
NM_004048.2:c.67+39C=	NP_004039.1:n.67+39C=
XM_005254549.2:c.67+39C=	XP_005254606.1:n.67+39C=
NM_004048.3:c.67+39C=	NP_004039.1:n.67+39C=
XM_005254549.3:c.67+39C=	XP_005254606.1:n.67+39C=
XR_002957658.1:n.122+39C=
NM_004048.4:c.67+39C= MANE Select	NP_004039.1:n.67+39C=