Canonical Allele Identifier: CA2628214406
Gene: B2M HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.44711436G>T , CM000677.2:g.44711436G>T GRCh38
NC_000015.9:g.45003634G>T , CM000677.1:g.45003634G>T GRCh37
NC_000015.8:g.42790926G>T NCBI36
NG_012920.1:g.4950G>T
NG_012920.2:g.4960G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000695792.1:n.79G>T