Canonical Allele Identifier: CA2628214420

Gene: B2M

Linked Data

• gnomAD v4: 15-44711454-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.44711454C>T , CM000677.2:g.44711454C>T	GRCh38
NC_000015.9:g.45003652C>T , CM000677.1:g.45003652C>T	GRCh37
NC_000015.8:g.42790944C>T	NCBI36
NG_012920.1:g.4968C>T
NG_012920.2:g.4978C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695792.1:n.83+14C>T