Canonical Allele Identifier: CA7536305

Gene: B2M

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.44715634T>C , CM000677.2:g.44715634T>C	GRCh38
NC_000015.9:g.45007832T>C , CM000677.1:g.45007832T>C	GRCh37
NC_000015.8:g.42795124T>C	NCBI36
NG_012920.1:g.9148T>C
NG_012920.2:g.9158T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000561139.2:c.135T>C	ENSP00000453186.1:p.Thr45=
ENST00000695792.1:n.295T>C
ENST00000648006.3:c.279T>C MANE Select	ENSP00000497910.1:p.Thr93=
ENST00000349264.10:c.146T>C	ENSP00000340858.6:p.Leu49Pro
ENST00000544417.5:c.225T>C	ENSP00000437604.2:p.Thr75=
ENST00000557901.5:c.*112T>C	ENSP00000452861.1:n.*112T>C
ENST00000558401.5:c.279T>C	ENSP00000452780.1:p.Thr93=
ENST00000559220.1:n.42+1086T>C
ENST00000559720.5:n.339T>C
ENST00000559907.5:n.306T>C
ENST00000559916.1:c.279T>C	ENSP00000453350.1:p.Thr93=
ENST00000560681.1:n.274T>C
ENST00000561139.1:c.135T>C	ENSP00000453186.1:p.Thr45=
ENST00000561424.5:c.279T>C	ENSP00000453191.1:p.Thr93=
NM_004048.2:c.279T>C	NP_004039.1:p.Thr93=
XM_005254549.2:c.279T>C	XP_005254606.1:p.Thr93=
NM_004048.3:c.279T>C	NP_004039.1:p.Thr93=
XM_005254549.3:c.279T>C	XP_005254606.1:p.Thr93=
XR_002957658.1:n.334T>C
NM_004048.4:c.279T>C MANE Select	NP_004039.1:p.Thr93=