Canonical Allele Identifier: CA2173753387

Gene: B2M

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.44711573G= , CM000677.2:g.44711573G=	GRCh38
NC_000015.9:g.45003771G= , CM000677.1:g.45003771G=	GRCh37
NC_000015.8:g.42791063G=	NCBI36
NG_012920.1:g.5087G=
NG_012920.2:g.5097G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695792.1:n.83+133G=
ENST00000648006.3:c.27G= MANE Select	ENSP00000497910.1:p.Val9=
ENST00000349264.10:c.27G=	ENSP00000340858.6:p.Val9=
ENST00000544417.5:c.27G=	ENSP00000437604.2:p.Val9=
ENST00000557901.5:c.27G=	ENSP00000452861.1:p.Val9=
ENST00000558401.5:c.27G=	ENSP00000452780.1:p.Val9=
ENST00000559720.5:n.87G=
ENST00000559916.1:c.27G=	ENSP00000453350.1:p.Val9=
ENST00000561424.5:c.27G=	ENSP00000453191.1:p.Val9=
NM_004048.2:c.27G=	NP_004039.1:p.Val9=
XM_005254549.2:c.27G=	XP_005254606.1:p.Val9=
NM_004048.3:c.27G=	NP_004039.1:p.Val9=
XM_005254549.3:c.27G=	XP_005254606.1:p.Val9=
XR_002957658.1:n.82G=
NM_004048.4:c.27G= MANE Select	NP_004039.1:p.Val9=