Canonical Allele Identifier: CA2173753319
Gene: B2M HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.44711480C= , CM000677.2:g.44711480C= GRCh38
NC_000015.9:g.45003678C= , CM000677.1:g.45003678C= GRCh37
NC_000015.8:g.42790970C= NCBI36
NG_012920.1:g.4994C=
NG_012920.2:g.5004C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000695792.1:n.83+40C=
ENST00000558401.5:c.-67C= ENSP00000452780.1:n.-67C=