Canonical Allele Identifier: CA2628214550

Gene: B2M

Linked Data

• gnomAD v4: 15-44711714-GTTCTC-G

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.44711715_44711719del , CM000677.2:g.44711715_44711719del	GRCh38
NC_000015.9:g.45003913_45003917del , CM000677.1:g.45003913_45003917del	GRCh37
NC_000015.8:g.42791205_42791209del	NCBI36
NG_012920.1:g.5229_5233del
NG_012920.2:g.5239_5243del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695792.1:n.83+275_83+279del
ENST00000648006.3:c.67+102_67+106del MANE Select	ENSP00000497910.1:n.67+102_67+106del
ENST00000349264.10:c.57+112_57+116del	ENSP00000340858.6:n.57+112_57+116del
ENST00000544417.5:c.67+102_67+106del	ENSP00000437604.2:n.67+102_67+106del
ENST00000557901.5:c.67+102_67+106del	ENSP00000452861.1:n.67+102_67+106del
ENST00000558401.5:c.67+102_67+106del	ENSP00000452780.1:n.67+102_67+106del
ENST00000559720.5:n.127+102_127+106del
ENST00000559916.1:c.67+102_67+106del	ENSP00000453350.1:n.67+102_67+106del
ENST00000561424.5:c.67+102_67+106del	ENSP00000453191.1:n.67+102_67+106del
NM_004048.2:c.67+102_67+106del	NP_004039.1:n.67+102_67+106del
XM_005254549.2:c.67+102_67+106del	XP_005254606.1:n.67+102_67+106del
NM_004048.3:c.67+102_67+106del	NP_004039.1:n.67+102_67+106del
XM_005254549.3:c.67+102_67+106del	XP_005254606.1:n.67+102_67+106del
XR_002957658.1:n.122+102_122+106del
NM_004048.4:c.67+102_67+106del MANE Select	NP_004039.1:n.67+102_67+106del