Canonical Allele Identifier: CA2173753383

Gene: B2M

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.44711566T= , CM000677.2:g.44711566T=	GRCh38
NC_000015.9:g.45003764T= , CM000677.1:g.45003764T=	GRCh37
NC_000015.8:g.42791056T=	NCBI36
NG_012920.1:g.5080T=
NG_012920.2:g.5090T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695792.1:n.83+126T=
ENST00000648006.3:c.20T= MANE Select	ENSP00000497910.1:p.Leu7=
ENST00000349264.10:c.20T=	ENSP00000340858.6:p.Leu7=
ENST00000544417.5:c.20T=	ENSP00000437604.2:p.Leu7=
ENST00000557901.5:c.20T=	ENSP00000452861.1:p.Leu7=
ENST00000558401.5:c.20T=	ENSP00000452780.1:p.Leu7=
ENST00000559720.5:n.80T=
ENST00000559916.1:c.20T=	ENSP00000453350.1:p.Leu7=
ENST00000561424.5:c.20T=	ENSP00000453191.1:p.Leu7=
NM_004048.2:c.20T=	NP_004039.1:p.Leu7=
XM_005254549.2:c.20T=	XP_005254606.1:p.Leu7=
NM_004048.3:c.20T=	NP_004039.1:p.Leu7=
XM_005254549.3:c.20T=	XP_005254606.1:p.Leu7=
XR_002957658.1:n.75T=
NM_004048.4:c.20T= MANE Select	NP_004039.1:p.Leu7=