Canonical Allele Identifier: CA2803979461

Gene: B2M

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.44711754_44711755insCCACCAAACCCAACCAAACACACCCAACAC , CM000677.2:g.44711754_44711755insCCACCAAACCCAACCAAACACACCCAACAC	GRCh38
NC_000015.9:g.45003952_45003953insCCACCAAACCCAACCAAACACACCCAACAC , CM000677.1:g.45003952_45003953insCCACCAAACCCAACCAAACACACCCAACAC	GRCh37
NC_000015.8:g.42791244_42791245insCCACCAAACCCAACCAAACACACCCAACAC	NCBI36
NG_012920.1:g.5268_5269insCCACCAAACCCAACCAAACACACCCAACAC
NG_012920.2:g.5278_5279insCCACCAAACCCAACCAAACACACCCAACAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695792.1:n.83+314_83+315insCCACCAAACCCAACCAAACACACCCAACAC
ENST00000648006.3:c.67+141_67+142insCCACCAAACCCAACCAAACACACCCAACAC MANE Select	ENSP00000497910.1:n.67+141_67+142insCCACCAAACCCAACCAAACACACCC...
ENST00000349264.10:c.57+151_57+152insCCACCAAACCCAACCAAACACACCCAACAC	ENSP00000340858.6:n.57+151_57+152insCCACCAAACCCAACCAAACACACCC...
ENST00000544417.5:c.67+141_67+142insCCACCAAACCCAACCAAACACACCCAACAC	ENSP00000437604.2:n.67+141_67+142insCCACCAAACCCAACCAAACACACCC...
ENST00000557901.5:c.67+141_67+142insCCACCAAACCCAACCAAACACACCCAACAC	ENSP00000452861.1:n.67+141_67+142insCCACCAAACCCAACCAAACACACCC...
ENST00000558401.5:c.67+141_67+142insCCACCAAACCCAACCAAACACACCCAACAC	ENSP00000452780.1:n.67+141_67+142insCCACCAAACCCAACCAAACACACCC...
ENST00000559720.5:n.127+141_127+142insCCACCAAACCCAACCAAACACACCCAACAC
ENST00000559916.1:c.67+141_67+142insCCACCAAACCCAACCAAACACACCCAACAC	ENSP00000453350.1:n.67+141_67+142insCCACCAAACCCAACCAAACACACCC...
ENST00000561424.5:c.67+141_67+142insCCACCAAACCCAACCAAACACACCCAACAC	ENSP00000453191.1:n.67+141_67+142insCCACCAAACCCAACCAAACACACCC...
NM_004048.2:c.67+141_67+142insCCACCAAACCCAACCAAACACACCCAACAC	NP_004039.1:n.67+141_67+142insCCACCAAACCCAACCAAACACACCCAACAC
XM_005254549.2:c.67+141_67+142insCCACCAAACCCAACCAAACACACCCAACAC	XP_005254606.1:n.67+141_67+142insCCACCAAACCCAACCAAACACACCCAAC...
NM_004048.3:c.67+141_67+142insCCACCAAACCCAACCAAACACACCCAACAC	NP_004039.1:n.67+141_67+142insCCACCAAACCCAACCAAACACACCCAACAC
XM_005254549.3:c.67+141_67+142insCCACCAAACCCAACCAAACACACCCAACAC	XP_005254606.1:n.67+141_67+142insCCACCAAACCCAACCAAACACACCCAAC...
XR_002957658.1:n.122+141_122+142insCCACCAAACCCAACCAAACACACCCAACAC
NM_004048.4:c.67+141_67+142insCCACCAAACCCAACCAAACACACCCAACAC MANE Select	NP_004039.1:n.67+141_67+142insCCACCAAACCCAACCAAACACACCCAACAC