Canonical Allele Identifier: CA618006585

Gene: B2M

Linked Data

• dbSNP Id: rs1348817182
• gnomAD v2: 15-45003881-GCT-G
• gnomAD v3: 15-44711683-GCT-G
• gnomAD v4: 15-44711683-GCT-G
• MyVariant Identifiers: chr15:g.45003882_45003883del (hg19) ; chr15:g.44711684_44711685del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.44711689_44711690del , CM000677.2:g.44711689_44711690del	GRCh38
NC_000015.9:g.45003887_45003888del , CM000677.1:g.45003887_45003888del	GRCh37
NC_000015.8:g.42791179_42791180del	NCBI36
NG_012920.1:g.5203_5204del
NG_012920.2:g.5213_5214del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695792.1:n.83+249_83+250del
ENST00000648006.3:c.67+76_67+77del MANE Select	ENSP00000497910.1:n.67+76_67+77del
ENST00000349264.10:c.57+86_57+87del	ENSP00000340858.6:n.57+86_57+87del
ENST00000544417.5:c.67+76_67+77del	ENSP00000437604.2:n.67+76_67+77del
ENST00000557901.5:c.67+76_67+77del	ENSP00000452861.1:n.67+76_67+77del
ENST00000558401.5:c.67+76_67+77del	ENSP00000452780.1:n.67+76_67+77del
ENST00000559720.5:n.127+76_127+77del
ENST00000559916.1:c.67+76_67+77del	ENSP00000453350.1:n.67+76_67+77del
ENST00000561424.5:c.67+76_67+77del	ENSP00000453191.1:n.67+76_67+77del
NM_004048.2:c.67+76_67+77del	NP_004039.1:n.67+76_67+77del
XM_005254549.2:c.67+76_67+77del	XP_005254606.1:n.67+76_67+77del
NM_004048.3:c.67+76_67+77del	NP_004039.1:n.67+76_67+77del
XM_005254549.3:c.67+76_67+77del	XP_005254606.1:n.67+76_67+77del
XR_002957658.1:n.122+76_122+77del
NM_004048.4:c.67+76_67+77del MANE Select	NP_004039.1:n.67+76_67+77del