Canonical Allele Identifier: CA618006544

Gene: B2M

Linked Data

• dbSNP Id: rs1416155278
• gnomAD v2: 15-45003678-C-T
• gnomAD v4: 15-44711480-C-T
• MyVariant Identifiers: chr15:g.45003678C>T (hg19) ; chr15:g.44711480C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.44711480C>T , CM000677.2:g.44711480C>T	GRCh38
NC_000015.9:g.45003678C>T , CM000677.1:g.45003678C>T	GRCh37
NC_000015.8:g.42790970C>T	NCBI36
NG_012920.1:g.4994C>T
NG_012920.2:g.5004C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695792.1:n.83+40C>T
ENST00000558401.5:c.-67C>T	ENSP00000452780.1:n.-67C>T