Canonical Allele Identifier: CA392232655

Gene: B2M

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.44715461G>A , CM000677.2:g.44715461G>A	GRCh38
NC_000015.9:g.45007659G>A , CM000677.1:g.45007659G>A	GRCh37
NC_000015.8:g.42794951G>A	NCBI36
NG_012920.1:g.8975G>A
NG_012920.2:g.8985G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695792.1:n.122G>A
ENST00000648006.3:c.106G>A MANE Select	ENSP00000497910.1:p.Glu36Lys
ENST00000349264.10:c.58-85G>A	ENSP00000340858.6:n.58-85G>A
ENST00000544417.5:c.103+3G>A	ENSP00000437604.2:n.103+3G>A
ENST00000557901.5:c.95G>A	ENSP00000452861.1:p.Arg32Lys
ENST00000558401.5:c.106G>A	ENSP00000452780.1:p.Glu36Lys
ENST00000559220.1:n.42+913G>A
ENST00000559720.5:n.166G>A
ENST00000559907.5:n.133G>A
ENST00000559916.1:c.106G>A	ENSP00000453350.1:p.Glu36Lys
ENST00000560681.1:n.101G>A
ENST00000561424.5:c.106G>A	ENSP00000453191.1:p.Glu36Lys
NM_004048.2:c.106G>A	NP_004039.1:p.Glu36Lys
XM_005254549.2:c.106G>A	XP_005254606.1:p.Glu36Lys
NM_004048.3:c.106G>A	NP_004039.1:p.Glu36Lys
XM_005254549.3:c.106G>A	XP_005254606.1:p.Glu36Lys
XR_002957658.1:n.161G>A
NM_004048.4:c.106G>A MANE Select	NP_004039.1:p.Glu36Lys