Canonical Allele Identifier: CA2628214536

Gene: B2M

Linked Data

• gnomAD v4: 15-44711703-CCCTTCT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.44711706_44711711del , CM000677.2:g.44711706_44711711del	GRCh38
NC_000015.9:g.45003904_45003909del , CM000677.1:g.45003904_45003909del	GRCh37
NC_000015.8:g.42791196_42791201del	NCBI36
NG_012920.1:g.5220_5225del
NG_012920.2:g.5230_5235del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695792.1:n.83+266_83+271del
ENST00000648006.3:c.67+93_67+98del MANE Select	ENSP00000497910.1:n.67+93_67+98del
ENST00000349264.10:c.57+103_57+108del	ENSP00000340858.6:n.57+103_57+108del
ENST00000544417.5:c.67+93_67+98del	ENSP00000437604.2:n.67+93_67+98del
ENST00000557901.5:c.67+93_67+98del	ENSP00000452861.1:n.67+93_67+98del
ENST00000558401.5:c.67+93_67+98del	ENSP00000452780.1:n.67+93_67+98del
ENST00000559720.5:n.127+93_127+98del
ENST00000559916.1:c.67+93_67+98del	ENSP00000453350.1:n.67+93_67+98del
ENST00000561424.5:c.67+93_67+98del	ENSP00000453191.1:n.67+93_67+98del
NM_004048.2:c.67+93_67+98del	NP_004039.1:n.67+93_67+98del
XM_005254549.2:c.67+93_67+98del	XP_005254606.1:n.67+93_67+98del
NM_004048.3:c.67+93_67+98del	NP_004039.1:n.67+93_67+98del
XM_005254549.3:c.67+93_67+98del	XP_005254606.1:n.67+93_67+98del
XR_002957658.1:n.122+93_122+98del
NM_004048.4:c.67+93_67+98del MANE Select	NP_004039.1:n.67+93_67+98del