Canonical Allele Identifier: CA2173753312
Gene: B2M HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.44711462G= , CM000677.2:g.44711462G= GRCh38
NC_000015.9:g.45003660G= , CM000677.1:g.45003660G= GRCh37
NC_000015.8:g.42790952G= NCBI36
NG_012920.1:g.4976G=
NG_012920.2:g.4986G=

Transcript Alleles

HGVS Amino-acid change
ENST00000695792.1:n.83+22G=