Canonical Allele Identifier: CA7536307

Gene: B2M

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.44715656C>T , CM000677.2:g.44715656C>T	GRCh38
NC_000015.9:g.45007854C>T , CM000677.1:g.45007854C>T	GRCh37
NC_000015.8:g.42795146C>T	NCBI36
NG_012920.1:g.9170C>T
NG_012920.2:g.9180C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000561139.2:c.157C>T	ENSP00000453186.1:p.Arg53Cys
ENST00000695792.1:n.317C>T
ENST00000648006.3:c.301C>T MANE Select	ENSP00000497910.1:p.Arg101Cys
ENST00000349264.10:c.168C>T	ENSP00000340858.6:p.Ala56=
ENST00000544417.5:c.247C>T	ENSP00000437604.2:p.Arg83Cys
ENST00000557901.5:c.*134C>T	ENSP00000452861.1:n.*134C>T
ENST00000558401.5:c.301C>T	ENSP00000452780.1:p.Arg101Cys
ENST00000559220.1:n.42+1108C>T
ENST00000559720.5:n.361C>T
ENST00000559907.5:n.328C>T
ENST00000559916.1:c.301C>T	ENSP00000453350.1:p.Arg101Cys
ENST00000560681.1:n.296C>T
ENST00000561139.1:c.157C>T	ENSP00000453186.1:p.Arg53Cys
ENST00000561424.5:c.301C>T	ENSP00000453191.1:p.Arg101Cys
NM_004048.2:c.301C>T	NP_004039.1:p.Arg101Cys
XM_005254549.2:c.301C>T	XP_005254606.1:p.Arg101Cys
NM_004048.3:c.301C>T	NP_004039.1:p.Arg101Cys
XM_005254549.3:c.301C>T	XP_005254606.1:p.Arg101Cys
XR_002957658.1:n.356C>T
NM_004048.4:c.301C>T MANE Select	NP_004039.1:p.Arg101Cys