Canonical Allele Identifier: CA2173753359

Gene: B2M

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.44711531C= , CM000677.2:g.44711531C=	GRCh38
NC_000015.9:g.45003729C= , CM000677.1:g.45003729C=	GRCh37
NC_000015.8:g.42791021C=	NCBI36
NG_012920.1:g.5045C=
NG_012920.2:g.5055C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695792.1:n.83+91C=
ENST00000648006.3:c.-16C= MANE Select	ENSP00000497910.1:n.-16C=
ENST00000349264.10:c.-16C=	ENSP00000340858.6:n.-16C=
ENST00000544417.5:c.-16C=	ENSP00000437604.2:n.-16C=
ENST00000557901.5:c.-16C=	ENSP00000452861.1:n.-16C=
ENST00000558401.5:c.-16C=	ENSP00000452780.1:n.-16C=
ENST00000559720.5:n.45C=
ENST00000559916.1:c.-16C=	ENSP00000453350.1:n.-16C=
ENST00000561424.5:c.-16C=	ENSP00000453191.1:n.-16C=
NM_004048.2:c.-16C=	NP_004039.1:n.-16C=
XM_005254549.2:c.-16C=	XP_005254606.1:n.-16C=
NM_004048.3:c.-16C=	NP_004039.1:n.-16C=
XM_005254549.3:c.-16C=	XP_005254606.1:n.-16C=
XR_002957658.1:n.40C=
NM_004048.4:c.-16C= MANE Select	NP_004039.1:n.-16C=