Canonical Allele Identifier: CA392232242

Gene: B2M

Linked Data

• MyVariant Identifiers: chr15:g.45003806T>C (hg19) ; chr15:g.44711608T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.44711608T>C , CM000677.2:g.44711608T>C	GRCh38
NC_000015.9:g.45003806T>C , CM000677.1:g.45003806T>C	GRCh37
NC_000015.8:g.42791098T>C	NCBI36
NG_012920.1:g.5122T>C
NG_012920.2:g.5132T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695792.1:n.83+168T>C
ENST00000648006.3:c.62T>C MANE Select	ENSP00000497910.1:p.Ile21Thr
ENST00000349264.10:c.57+5T>C	ENSP00000340858.6:n.57+5T>C
ENST00000544417.5:c.62T>C	ENSP00000437604.2:p.Ile21Thr
ENST00000557901.5:c.62T>C	ENSP00000452861.1:p.Ile21Thr
ENST00000558401.5:c.62T>C	ENSP00000452780.1:p.Ile21Thr
ENST00000559720.5:n.122T>C
ENST00000559916.1:c.62T>C	ENSP00000453350.1:p.Ile21Thr
ENST00000561424.5:c.62T>C	ENSP00000453191.1:p.Ile21Thr
NM_004048.2:c.62T>C	NP_004039.1:p.Ile21Thr
XM_005254549.2:c.62T>C	XP_005254606.1:p.Ile21Thr
NM_004048.3:c.62T>C	NP_004039.1:p.Ile21Thr
XM_005254549.3:c.62T>C	XP_005254606.1:p.Ile21Thr
XR_002957658.1:n.117T>C
NM_004048.4:c.62T>C MANE Select	NP_004039.1:p.Ile21Thr