Canonical Allele Identifier: CA2173753313
Gene: B2M HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.44711463T= , CM000677.2:g.44711463T= GRCh38
NC_000015.9:g.45003661T= , CM000677.1:g.45003661T= GRCh37
NC_000015.8:g.42790953T= NCBI36
NG_012920.1:g.4977T=
NG_012920.2:g.4987T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000695792.1:n.83+23T=