Canonical Allele Identifier: CA2173753403

Gene: B2M

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.44711609C= , CM000677.2:g.44711609C=	GRCh38
NC_000015.9:g.45003807C= , CM000677.1:g.45003807C=	GRCh37
NC_000015.8:g.42791099C=	NCBI36
NG_012920.1:g.5123C=
NG_012920.2:g.5133C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695792.1:n.83+169C=
ENST00000648006.3:c.63C= MANE Select	ENSP00000497910.1:p.Ile21=
ENST00000349264.10:c.57+6C=	ENSP00000340858.6:n.57+6C=
ENST00000544417.5:c.63C=	ENSP00000437604.2:p.Ile21=
ENST00000557901.5:c.63C=	ENSP00000452861.1:p.Ile21=
ENST00000558401.5:c.63C=	ENSP00000452780.1:p.Ile21=
ENST00000559720.5:n.123C=
ENST00000559916.1:c.63C=	ENSP00000453350.1:p.Ile21=
ENST00000561424.5:c.63C=	ENSP00000453191.1:p.Ile21=
NM_004048.2:c.63C=	NP_004039.1:p.Ile21=
XM_005254549.2:c.63C=	XP_005254606.1:p.Ile21=
NM_004048.3:c.63C=	NP_004039.1:p.Ile21=
XM_005254549.3:c.63C=	XP_005254606.1:p.Ile21=
XR_002957658.1:n.118C=
NM_004048.4:c.63C= MANE Select	NP_004039.1:p.Ile21=