Canonical Allele Identifier: CA2628214394
Gene: B2M HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.44711426C>A , CM000677.2:g.44711426C>A GRCh38
NC_000015.9:g.45003624C>A , CM000677.1:g.45003624C>A GRCh37
NC_000015.8:g.42790916C>A NCBI36
NG_012920.1:g.4940C>A
NG_012920.2:g.4950C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000695792.1:n.69C>A