Canonical Allele Identifier: CA2173753348

Gene: B2M

Linked Data

• dbSNP Id: rs2086863311

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.44711517A>G , CM000677.2:g.44711517A>G	GRCh38
NC_000015.9:g.45003715A>G , CM000677.1:g.45003715A>G	GRCh37
NC_000015.8:g.42791007A>G	NCBI36
NG_012920.1:g.5031A>G
NG_012920.2:g.5041A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695792.1:n.83+77A>G
ENST00000648006.3:c.-30A>G MANE Select	ENSP00000497910.1:n.-30A>G
ENST00000349264.10:c.-30A>G	ENSP00000340858.6:n.-30A>G
ENST00000544417.5:c.-30A>G	ENSP00000437604.2:n.-30A>G
ENST00000558401.5:c.-30A>G	ENSP00000452780.1:n.-30A>G
ENST00000559720.5:n.31A>G
ENST00000559916.1:c.-30A>G	ENSP00000453350.1:n.-30A>G
ENST00000561424.5:c.-30A>G	ENSP00000453191.1:n.-30A>G
NM_004048.2:c.-30A>G	NP_004039.1:n.-30A>G
XM_005254549.2:c.-30A>G	XP_005254606.1:n.-30A>G
NM_004048.3:c.-30A>G	NP_004039.1:n.-30A>G
XM_005254549.3:c.-30A>G	XP_005254606.1:n.-30A>G
XR_002957658.1:n.26A>G
NM_004048.4:c.-30A>G MANE Select	NP_004039.1:n.-30A>G