Canonical Allele Identifier: CA270116950

Gene: B2M

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.44715449C>T , CM000677.2:g.44715449C>T	GRCh38
NC_000015.9:g.45007647C>T , CM000677.1:g.45007647C>T	GRCh37
NC_000015.8:g.42794939C>T	NCBI36
NG_012920.1:g.8963C>T
NG_012920.2:g.8973C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695792.1:n.110C>T
ENST00000648006.3:c.94C>T MANE Select	ENSP00000497910.1:p.Arg32Cys
ENST00000349264.10:c.58-97C>T	ENSP00000340858.6:n.58-97C>T
ENST00000544417.5:c.94C>T	ENSP00000437604.2:p.Arg32Cys
ENST00000557901.5:c.83C>T	ENSP00000452861.1:p.Thr28Met
ENST00000558401.5:c.94C>T	ENSP00000452780.1:p.Arg32Cys
ENST00000559220.1:n.42+901C>T
ENST00000559720.5:n.154C>T
ENST00000559907.5:n.121C>T
ENST00000559916.1:c.94C>T	ENSP00000453350.1:p.Arg32Cys
ENST00000560681.1:n.89C>T
ENST00000561424.5:c.94C>T	ENSP00000453191.1:p.Arg32Cys
NM_004048.2:c.94C>T	NP_004039.1:p.Arg32Cys
XM_005254549.2:c.94C>T	XP_005254606.1:p.Arg32Cys
NM_004048.3:c.94C>T	NP_004039.1:p.Arg32Cys
XM_005254549.3:c.94C>T	XP_005254606.1:p.Arg32Cys
XR_002957658.1:n.149C>T
NM_004048.4:c.94C>T MANE Select	NP_004039.1:p.Arg32Cys