Canonical Allele Identifier: CA270114147

Gene: B2M

Linked Data

• dbSNP Id: rs974572986
• MyVariant Identifiers: chr15:g.44711455G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.44711455G>C , CM000677.2:g.44711455G>C	GRCh38
NC_000015.9:g.45003653G>C , CM000677.1:g.45003653G>C	GRCh37
NC_000015.8:g.42790945G>C	NCBI36
NG_012920.1:g.4969G>C
NG_012920.2:g.4979G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695792.1:n.83+15G>C