Canonical Allele Identifier: CA7536290

Gene: B2M

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.44715502G>A , CM000677.2:g.44715502G>A	GRCh38
NC_000015.9:g.45007700G>A , CM000677.1:g.45007700G>A	GRCh37
NC_000015.8:g.42794992G>A	NCBI36
NG_012920.1:g.9016G>A
NG_012920.2:g.9026G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000561139.2:c.3G>A	ENSP00000453186.1:p.Gly1=
ENST00000695792.1:n.163G>A
ENST00000648006.3:c.147G>A MANE Select	ENSP00000497910.1:p.Gly49=
ENST00000349264.10:c.58-44G>A	ENSP00000340858.6:n.58-44G>A
ENST00000544417.5:c.104-11G>A	ENSP00000437604.2:n.104-11G>A
ENST00000557901.5:c.136G>A	ENSP00000452861.1:p.Val46Ile
ENST00000558401.5:c.147G>A	ENSP00000452780.1:p.Gly49=
ENST00000559220.1:n.42+954G>A
ENST00000559720.5:n.207G>A
ENST00000559907.5:n.174G>A
ENST00000559916.1:c.147G>A	ENSP00000453350.1:p.Gly49=
ENST00000560681.1:n.142G>A
ENST00000561139.1:c.3G>A	ENSP00000453186.1:p.Gly1=
ENST00000561424.5:c.147G>A	ENSP00000453191.1:p.Gly49=
NM_004048.2:c.147G>A	NP_004039.1:p.Gly49=
XM_005254549.2:c.147G>A	XP_005254606.1:p.Gly49=
NM_004048.3:c.147G>A	NP_004039.1:p.Gly49=
XM_005254549.3:c.147G>A	XP_005254606.1:p.Gly49=
XR_002957658.1:n.202G>A
NM_004048.4:c.147G>A MANE Select	NP_004039.1:p.Gly49=