Canonical Allele Identifier: CA490206946

Gene: B2M

Linked Data

• MyVariant Identifiers: chr15:g.45003804T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.44711606T>G , CM000677.2:g.44711606T>G	GRCh38
NC_000015.9:g.45003804T>G , CM000677.1:g.45003804T>G	GRCh37
NC_000015.8:g.42791096T>G	NCBI36
NG_012920.1:g.5120T>G
NG_012920.2:g.5130T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695792.1:n.83+166T>G
ENST00000648006.3:c.60T>G MANE Select	ENSP00000497910.1:p.Ala20=
ENST00000349264.10:c.57+3T>G	ENSP00000340858.6:n.57+3T>G
ENST00000544417.5:c.60T>G	ENSP00000437604.2:p.Ala20=
ENST00000557901.5:c.60T>G	ENSP00000452861.1:p.Ala20=
ENST00000558401.5:c.60T>G	ENSP00000452780.1:p.Ala20=
ENST00000559720.5:n.120T>G
ENST00000559916.1:c.60T>G	ENSP00000453350.1:p.Ala20=
ENST00000561424.5:c.60T>G	ENSP00000453191.1:p.Ala20=
NM_004048.2:c.60T>G	NP_004039.1:p.Ala20=
XM_005254549.2:c.60T>G	XP_005254606.1:p.Ala20=
NM_004048.3:c.60T>G	NP_004039.1:p.Ala20=
XM_005254549.3:c.60T>G	XP_005254606.1:p.Ala20=
XR_002957658.1:n.115T>G
NM_004048.4:c.60T>G MANE Select	NP_004039.1:p.Ala20=