Canonical Allele Identifier: CA2730858798
Gene: B2M HGNC NCBI

Linked Data

dbSNP Id: rs2141284121

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.44711477del , CM000677.2:g.44711477del GRCh38
NC_000015.9:g.45003675del , CM000677.1:g.45003675del GRCh37
NC_000015.8:g.42790967del NCBI36
NG_012920.1:g.4991del
NG_012920.2:g.5001del

Transcript Alleles

HGVS Amino-acid Change
ENST00000695792.1:n.83+37del