Canonical Allele Identifier: CA490206939

Gene: B2M

Linked Data

• MyVariant Identifiers: chr15:g.45003796C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.44711598C>T , CM000677.2:g.44711598C>T	GRCh38
NC_000015.9:g.45003796C>T , CM000677.1:g.45003796C>T	GRCh37
NC_000015.8:g.42791088C>T	NCBI36
NG_012920.1:g.5112C>T
NG_012920.2:g.5122C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695792.1:n.83+158C>T
ENST00000648006.3:c.52C>T MANE Select	ENSP00000497910.1:p.Leu18=
ENST00000349264.10:c.52C>T	ENSP00000340858.6:p.Leu18=
ENST00000544417.5:c.52C>T	ENSP00000437604.2:p.Leu18=
ENST00000557901.5:c.52C>T	ENSP00000452861.1:p.Leu18=
ENST00000558401.5:c.52C>T	ENSP00000452780.1:p.Leu18=
ENST00000559720.5:n.112C>T
ENST00000559916.1:c.52C>T	ENSP00000453350.1:p.Leu18=
ENST00000561424.5:c.52C>T	ENSP00000453191.1:p.Leu18=
NM_004048.2:c.52C>T	NP_004039.1:p.Leu18=
XM_005254549.2:c.52C>T	XP_005254606.1:p.Leu18=
NM_004048.3:c.52C>T	NP_004039.1:p.Leu18=
XM_005254549.3:c.52C>T	XP_005254606.1:p.Leu18=
XR_002957658.1:n.107C>T
NM_004048.4:c.52C>T MANE Select	NP_004039.1:p.Leu18=