Canonical Allele Identifier: CA969306715
Gene: B2M HGNC NCBI

Linked Data

dbSNP Id: rs1595996261

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.44711424C>A , CM000677.2:g.44711424C>A GRCh38
NC_000015.9:g.45003622C>A , CM000677.1:g.45003622C>A GRCh37
NC_000015.8:g.42790914C>A NCBI36
NG_012920.1:g.4938C>A
NG_012920.2:g.4948C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000695792.1:n.67C>A