Canonical Allele Identifier: CA713086666

Gene: B2M

Linked Data

• dbSNP Id: rs1221862664
• gnomAD v3: 15-44711739-GC-G
• gnomAD v4: 15-44711739-GC-G
• MyVariant Identifiers: chr15:g.45003938del (hg19) ; chr15:g.44711740del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.44711740del , CM000677.2:g.44711740del	GRCh38
NC_000015.9:g.45003938del , CM000677.1:g.45003938del	GRCh37
NC_000015.8:g.42791230del	NCBI36
NG_012920.1:g.5254del
NG_012920.2:g.5264del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695792.1:n.83+300del
ENST00000648006.3:c.67+127del MANE Select	ENSP00000497910.1:n.67+127del
ENST00000349264.10:c.57+137del	ENSP00000340858.6:n.57+137del
ENST00000544417.5:c.67+127del	ENSP00000437604.2:n.67+127del
ENST00000557901.5:c.67+127del	ENSP00000452861.1:n.67+127del
ENST00000558401.5:c.67+127del	ENSP00000452780.1:n.67+127del
ENST00000559720.5:n.127+127del
ENST00000559916.1:c.67+127del	ENSP00000453350.1:n.67+127del
ENST00000561424.5:c.67+127del	ENSP00000453191.1:n.67+127del
NM_004048.2:c.67+127del	NP_004039.1:n.67+127del
XM_005254549.2:c.67+127del	XP_005254606.1:n.67+127del
NM_004048.3:c.67+127del	NP_004039.1:n.67+127del
XM_005254549.3:c.67+127del	XP_005254606.1:n.67+127del
XR_002957658.1:n.122+127del
NM_004048.4:c.67+127del MANE Select	NP_004039.1:n.67+127del