Canonical Allele Identifier: CA2575709653
Gene: B2M HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.44711459C>G , CM000677.2:g.44711459C>G GRCh38
NC_000015.9:g.45003657C>G , CM000677.1:g.45003657C>G GRCh37
NC_000015.8:g.42790949C>G NCBI36
NG_012920.1:g.4973C>G
NG_012920.2:g.4983C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000695792.1:n.83+19C>G