Canonical Allele Identifier: CA2173753317
Gene: B2M HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.44711479A= , CM000677.2:g.44711479A= GRCh38
NC_000015.9:g.45003677A= , CM000677.1:g.45003677A= GRCh37
NC_000015.8:g.42790969A= NCBI36
NG_012920.1:g.4993A=
NG_012920.2:g.5003A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000695792.1:n.83+39A=
ENST00000558401.5:c.-68A= ENSP00000452780.1:n.-68A=