Canonical Allele Identifier: CA490330725

Gene: B2M

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.44715655C>T , CM000677.2:g.44715655C>T	GRCh38
NC_000015.9:g.45007853C>T , CM000677.1:g.45007853C>T	GRCh37
NC_000015.8:g.42795145C>T	NCBI36
NG_012920.1:g.9169C>T
NG_012920.2:g.9179C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000561139.2:c.156C>T	ENSP00000453186.1:p.Cys52=
ENST00000695792.1:n.316C>T
ENST00000648006.3:c.300C>T MANE Select	ENSP00000497910.1:p.Cys100=
ENST00000349264.10:c.167C>T	ENSP00000340858.6:p.Ala56Val
ENST00000544417.5:c.246C>T	ENSP00000437604.2:p.Cys82=
ENST00000557901.5:c.*133C>T	ENSP00000452861.1:n.*133C>T
ENST00000558401.5:c.300C>T	ENSP00000452780.1:p.Cys100=
ENST00000559220.1:n.42+1107C>T
ENST00000559720.5:n.360C>T
ENST00000559907.5:n.327C>T
ENST00000559916.1:c.300C>T	ENSP00000453350.1:p.Cys100=
ENST00000560681.1:n.295C>T
ENST00000561139.1:c.156C>T	ENSP00000453186.1:p.Cys52=
ENST00000561424.5:c.300C>T	ENSP00000453191.1:p.Cys100=
NM_004048.2:c.300C>T	NP_004039.1:p.Cys100=
XM_005254549.2:c.300C>T	XP_005254606.1:p.Cys100=
NM_004048.3:c.300C>T	NP_004039.1:p.Cys100=
XM_005254549.3:c.300C>T	XP_005254606.1:p.Cys100=
XR_002957658.1:n.355C>T
NM_004048.4:c.300C>T MANE Select	NP_004039.1:p.Cys100=