Canonical Allele Identifier: CA2628214552

Gene: B2M

Linked Data

• gnomAD v4: 15-44711716-TCTC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.44711719_44711721del , CM000677.2:g.44711719_44711721del	GRCh38
NC_000015.9:g.45003917_45003919del , CM000677.1:g.45003917_45003919del	GRCh37
NC_000015.8:g.42791209_42791211del	NCBI36
NG_012920.1:g.5233_5235del
NG_012920.2:g.5243_5245del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695792.1:n.83+279_83+281del
ENST00000648006.3:c.67+106_67+108del MANE Select	ENSP00000497910.1:n.67+106_67+108del
ENST00000349264.10:c.57+116_57+118del	ENSP00000340858.6:n.57+116_57+118del
ENST00000544417.5:c.67+106_67+108del	ENSP00000437604.2:n.67+106_67+108del
ENST00000557901.5:c.67+106_67+108del	ENSP00000452861.1:n.67+106_67+108del
ENST00000558401.5:c.67+106_67+108del	ENSP00000452780.1:n.67+106_67+108del
ENST00000559720.5:n.127+106_127+108del
ENST00000559916.1:c.67+106_67+108del	ENSP00000453350.1:n.67+106_67+108del
ENST00000561424.5:c.67+106_67+108del	ENSP00000453191.1:n.67+106_67+108del
NM_004048.2:c.67+106_67+108del	NP_004039.1:n.67+106_67+108del
XM_005254549.2:c.67+106_67+108del	XP_005254606.1:n.67+106_67+108del
NM_004048.3:c.67+106_67+108del	NP_004039.1:n.67+106_67+108del
XM_005254549.3:c.67+106_67+108del	XP_005254606.1:n.67+106_67+108del
XR_002957658.1:n.122+106_122+108del
NM_004048.4:c.67+106_67+108del MANE Select	NP_004039.1:n.67+106_67+108del