Canonical Allele Identifier: CA16602808
Gene: B2M HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 376369
dbSNP Id: rs1023835002

User contributed link-outs

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.44711547A>G , CM000677.2:g.44711547A>G GRCh38
NC_000015.9:g.45003745A>G , CM000677.1:g.45003745A>G GRCh37
NC_000015.8:g.42791037A>G NCBI36
NG_012920.1:g.5061A>G
NG_012920.2:g.5071A>G

Transcript Alleles

HGVS Amino-acid change
NM_004048.2:c.1A>G VV
XM_005254549.2:c.1A>G
NM_004048.3:c.1A>G VV
XM_005254549.3:c.1A>G
XR_002957658.1:n.56A>G
ENST00000349264.10:c.1A>G
ENST00000544417.5:c.1A>G
ENST00000557901.5:c.1A>G
ENST00000558401.5:c.1A>G
ENST00000559720.5:n.61A>G
ENST00000559916.1:c.1A>G
ENST00000561424.5:c.1A>G