Canonical Allele Identifier: CA490206917

Gene: B2M

Linked Data

• dbSNP Id: rs552741313
• gnomAD v2: 15-45003771-G-T
• gnomAD v4: 15-44711573-G-T
• MyVariant Identifiers: chr15:g.45003771G>T (hg19) ; chr15:g.44711573G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.44711573G>T , CM000677.2:g.44711573G>T	GRCh38
NC_000015.9:g.45003771G>T , CM000677.1:g.45003771G>T	GRCh37
NC_000015.8:g.42791063G>T	NCBI36
NG_012920.1:g.5087G>T
NG_012920.2:g.5097G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695792.1:n.83+133G>T
ENST00000648006.3:c.27G>T MANE Select	ENSP00000497910.1:p.Val9=
ENST00000349264.10:c.27G>T	ENSP00000340858.6:p.Val9=
ENST00000544417.5:c.27G>T	ENSP00000437604.2:p.Val9=
ENST00000557901.5:c.27G>T	ENSP00000452861.1:p.Val9=
ENST00000558401.5:c.27G>T	ENSP00000452780.1:p.Val9=
ENST00000559720.5:n.87G>T
ENST00000559916.1:c.27G>T	ENSP00000453350.1:p.Val9=
ENST00000561424.5:c.27G>T	ENSP00000453191.1:p.Val9=
NM_004048.2:c.27G>T	NP_004039.1:p.Val9=
XM_005254549.2:c.27G>T	XP_005254606.1:p.Val9=
NM_004048.3:c.27G>T	NP_004039.1:p.Val9=
XM_005254549.3:c.27G>T	XP_005254606.1:p.Val9=
XR_002957658.1:n.82G>T
NM_004048.4:c.27G>T MANE Select	NP_004039.1:p.Val9=