Canonical Allele Identifier: CA2173753320
Gene: B2M HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.44711483G= , CM000677.2:g.44711483G= GRCh38
NC_000015.9:g.45003681G= , CM000677.1:g.45003681G= GRCh37
NC_000015.8:g.42790973G= NCBI36
NG_012920.1:g.4997G=
NG_012920.2:g.5007G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000695792.1:n.83+43G=
ENST00000558401.5:c.-64G= ENSP00000452780.1:n.-64G=