Canonical Allele Identifier: CA392232249

Gene: B2M

Linked Data

• dbSNP Id: rs1213728428
• gnomAD v2: 15-45003809-A-G
• gnomAD v4: 15-44711611-A-G
• MyVariant Identifiers: chr15:g.45003809A>G (hg19) ; chr15:g.44711611A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.44711611A>G , CM000677.2:g.44711611A>G	GRCh38
NC_000015.9:g.45003809A>G , CM000677.1:g.45003809A>G	GRCh37
NC_000015.8:g.42791101A>G	NCBI36
NG_012920.1:g.5125A>G
NG_012920.2:g.5135A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695792.1:n.83+171A>G
ENST00000648006.3:c.65A>G MANE Select	ENSP00000497910.1:p.Gln22Arg
ENST00000349264.10:c.57+8A>G	ENSP00000340858.6:n.57+8A>G
ENST00000544417.5:c.65A>G	ENSP00000437604.2:p.Gln22Arg
ENST00000557901.5:c.65A>G	ENSP00000452861.1:p.Gln22Arg
ENST00000558401.5:c.65A>G	ENSP00000452780.1:p.Gln22Arg
ENST00000559720.5:n.125A>G
ENST00000559916.1:c.65A>G	ENSP00000453350.1:p.Gln22Arg
ENST00000561424.5:c.65A>G	ENSP00000453191.1:p.Gln22Arg
NM_004048.2:c.65A>G	NP_004039.1:p.Gln22Arg
XM_005254549.2:c.65A>G	XP_005254606.1:p.Gln22Arg
NM_004048.3:c.65A>G	NP_004039.1:p.Gln22Arg
XM_005254549.3:c.65A>G	XP_005254606.1:p.Gln22Arg
XR_002957658.1:n.120A>G
NM_004048.4:c.65A>G MANE Select	NP_004039.1:p.Gln22Arg