Canonical Allele Identifier: CA2628214432
Gene: B2M HGNC NCBI

Linked Data

gnomAD v4: 15-44711470-T-A
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.44711470T>A , CM000677.2:g.44711470T>A GRCh38
NC_000015.9:g.45003668T>A , CM000677.1:g.45003668T>A GRCh37
NC_000015.8:g.42790960T>A NCBI36
NG_012920.1:g.4984T>A
NG_012920.2:g.4994T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000695792.1:n.83+30T>A
Search 100 bp 5'
Search 100 bp 3'