Canonical Allele Identifier: CA7536293

Gene: B2M

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.44715515G>A , CM000677.2:g.44715515G>A	GRCh38
NC_000015.9:g.45007713G>A , CM000677.1:g.45007713G>A	GRCh37
NC_000015.8:g.42795005G>A	NCBI36
NG_012920.1:g.9029G>A
NG_012920.2:g.9039G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_004048.4:c.160G>A MANE Select	NP_004039.1:p.Asp54Asn
ENST00000648006.3:c.160G>A MANE Select	ENSP00000497910.1:p.Asp54Asn
NM_004048.2:c.160G>A	NP_004039.1:p.Asp54Asn
NM_004048.3:c.160G>A	NP_004039.1:p.Asp54Asn
ENST00000349264.10:c.58-31G>A	ENSP00000340858.6:n.58-31G>A
ENST00000544417.5:c.106G>A	ENSP00000437604.2:p.Asp36Asn
ENST00000557901.5:c.149G>A	ENSP00000452861.1:p.Arg50Gln
ENST00000558401.5:c.160G>A	ENSP00000452780.1:p.Asp54Asn
ENST00000559220.1:n.42+967G>A
ENST00000559720.5:n.220G>A
ENST00000559907.5:n.187G>A
ENST00000559916.1:c.160G>A	ENSP00000453350.1:p.Asp54Asn
ENST00000560681.1:n.155G>A
ENST00000561139.1:c.16G>A	ENSP00000453186.1:p.Asp6Asn
ENST00000561139.2:c.16G>A	ENSP00000453186.1:p.Asp6Asn
ENST00000561424.5:c.160G>A	ENSP00000453191.1:p.Asp54Asn
ENST00000695792.1:n.176G>A
XM_005254549.2:c.160G>A	XP_005254606.1:p.Asp54Asn
XM_005254549.3:c.160G>A	XP_005254606.1:p.Asp54Asn
XR_002957658.1:n.215G>A