Canonical Allele Identifier: CA2628214436
Gene: B2M HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.44711472G>T , CM000677.2:g.44711472G>T GRCh38
NC_000015.9:g.45003670G>T , CM000677.1:g.45003670G>T GRCh37
NC_000015.8:g.42790962G>T NCBI36
NG_012920.1:g.4986G>T
NG_012920.2:g.4996G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000695792.1:n.83+32G>T