Canonical Allele Identifier: CA2173753293
Gene: B2M HGNC NCBI

Genomic Alleles

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

Transcript Alleles

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