Canonical Allele Identifier: CA2730861326

Gene: B2M

Linked Data

• dbSNP Id: rs2141284961

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.44711685_44711686insTC , CM000677.2:g.44711685_44711686insTC	GRCh38
NC_000015.9:g.45003883_45003884insTC , CM000677.1:g.45003883_45003884insTC	GRCh37
NC_000015.8:g.42791175_42791176insTC	NCBI36
NG_012920.1:g.5199_5200insTC
NG_012920.2:g.5209_5210insTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695792.1:n.83+245_83+246insTC
ENST00000648006.3:c.67+72_67+73insTC MANE Select	ENSP00000497910.1:n.67+72_67+73insTC
ENST00000349264.10:c.57+82_57+83insTC	ENSP00000340858.6:n.57+82_57+83insTC
ENST00000544417.5:c.67+72_67+73insTC	ENSP00000437604.2:n.67+72_67+73insTC
ENST00000557901.5:c.67+72_67+73insTC	ENSP00000452861.1:n.67+72_67+73insTC
ENST00000558401.5:c.67+72_67+73insTC	ENSP00000452780.1:n.67+72_67+73insTC
ENST00000559720.5:n.127+72_127+73insTC
ENST00000559916.1:c.67+72_67+73insTC	ENSP00000453350.1:n.67+72_67+73insTC
ENST00000561424.5:c.67+72_67+73insTC	ENSP00000453191.1:n.67+72_67+73insTC
NM_004048.2:c.67+72_67+73insTC	NP_004039.1:n.67+72_67+73insTC
XM_005254549.2:c.67+72_67+73insTC	XP_005254606.1:n.67+72_67+73insTC
NM_004048.3:c.67+72_67+73insTC	NP_004039.1:n.67+72_67+73insTC
XM_005254549.3:c.67+72_67+73insTC	XP_005254606.1:n.67+72_67+73insTC
XR_002957658.1:n.122+72_122+73insTC
NM_004048.4:c.67+72_67+73insTC MANE Select	NP_004039.1:n.67+72_67+73insTC