Canonical Allele Identifier: CA2173753308
Gene: B2M HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.44711454C= , CM000677.2:g.44711454C= GRCh38
NC_000015.9:g.45003652C= , CM000677.1:g.45003652C= GRCh37
NC_000015.8:g.42790944C= NCBI36
NG_012920.1:g.4968C=
NG_012920.2:g.4978C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000695792.1:n.83+14C=