Canonical Allele Identifier: CA270114179

Gene: B2M

Linked Data

• dbSNP Id: rs113663466
• MyVariant Identifiers: chr15:g.45003710C>G (hg19) ; chr15:g.44711512C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.44711512C>G , CM000677.2:g.44711512C>G	GRCh38
NC_000015.9:g.45003710C>G , CM000677.1:g.45003710C>G	GRCh37
NC_000015.8:g.42791002C>G	NCBI36
NG_012920.1:g.5026C>G
NG_012920.2:g.5036C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695792.1:n.83+72C>G
ENST00000544417.5:c.-35C>G	ENSP00000437604.2:n.-35C>G
ENST00000558401.5:c.-35C>G	ENSP00000452780.1:n.-35C>G
ENST00000559720.5:n.26C>G
ENST00000561424.5:c.-35C>G	ENSP00000453191.1:n.-35C>G
NM_004048.2:c.-35C>G	NP_004039.1:n.-35C>G
XM_005254549.2:c.-35C>G	XP_005254606.1:n.-35C>G
XM_005254549.3:c.-35C>G	XP_005254606.1:n.-35C>G
XR_002957658.1:n.21C>G