Canonical Allele Identifier: CA2628214423
Gene: B2M HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.44711458C>T , CM000677.2:g.44711458C>T GRCh38
NC_000015.9:g.45003656C>T , CM000677.1:g.45003656C>T GRCh37
NC_000015.8:g.42790948C>T NCBI36
NG_012920.1:g.4972C>T
NG_012920.2:g.4982C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000695792.1:n.83+18C>T