Canonical Allele Identifier: CA392232236

Gene: B2M

Linked Data

• MyVariant Identifiers: chr15:g.45003803C>A (hg19) ; chr15:g.44711605C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.44711605C>A , CM000677.2:g.44711605C>A	GRCh38
NC_000015.9:g.45003803C>A , CM000677.1:g.45003803C>A	GRCh37
NC_000015.8:g.42791095C>A	NCBI36
NG_012920.1:g.5119C>A
NG_012920.2:g.5129C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695792.1:n.83+165C>A
ENST00000648006.3:c.59C>A MANE Select	ENSP00000497910.1:p.Ala20Asp
ENST00000349264.10:c.57+2C>A	ENSP00000340858.6:n.57+2C>A
ENST00000544417.5:c.59C>A	ENSP00000437604.2:p.Ala20Asp
ENST00000557901.5:c.59C>A	ENSP00000452861.1:p.Ala20Asp
ENST00000558401.5:c.59C>A	ENSP00000452780.1:p.Ala20Asp
ENST00000559720.5:n.119C>A
ENST00000559916.1:c.59C>A	ENSP00000453350.1:p.Ala20Asp
ENST00000561424.5:c.59C>A	ENSP00000453191.1:p.Ala20Asp
NM_004048.2:c.59C>A	NP_004039.1:p.Ala20Asp
XM_005254549.2:c.59C>A	XP_005254606.1:p.Ala20Asp
NM_004048.3:c.59C>A	NP_004039.1:p.Ala20Asp
XM_005254549.3:c.59C>A	XP_005254606.1:p.Ala20Asp
XR_002957658.1:n.114C>A
NM_004048.4:c.59C>A MANE Select	NP_004039.1:p.Ala20Asp