Canonical Allele Identifier: CA2173753401

Gene: B2M

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.44711596G= , CM000677.2:g.44711596G=	GRCh38
NC_000015.9:g.45003794G= , CM000677.1:g.45003794G=	GRCh37
NC_000015.8:g.42791086G=	NCBI36
NG_012920.1:g.5110G=
NG_012920.2:g.5120G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695792.1:n.83+156G=
ENST00000648006.3:c.50G= MANE Select	ENSP00000497910.1:p.Gly17=
ENST00000349264.10:c.50G=	ENSP00000340858.6:p.Gly17=
ENST00000544417.5:c.50G=	ENSP00000437604.2:p.Gly17=
ENST00000557901.5:c.50G=	ENSP00000452861.1:p.Gly17=
ENST00000558401.5:c.50G=	ENSP00000452780.1:p.Gly17=
ENST00000559720.5:n.110G=
ENST00000559916.1:c.50G=	ENSP00000453350.1:p.Gly17=
ENST00000561424.5:c.50G=	ENSP00000453191.1:p.Gly17=
NM_004048.2:c.50G=	NP_004039.1:p.Gly17=
XM_005254549.2:c.50G=	XP_005254606.1:p.Gly17=
NM_004048.3:c.50G=	NP_004039.1:p.Gly17=
XM_005254549.3:c.50G=	XP_005254606.1:p.Gly17=
XR_002957658.1:n.105G=
NM_004048.4:c.50G= MANE Select	NP_004039.1:p.Gly17=