Canonical Allele Identifier: CA392232249
Gene: B2M HGNC NCBI

Linked Data

dbSNP Id: rs1213728428

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