Canonical Allele Identifier: CA7536263

Gene: B2M

Linked Data

• ClinVar Variation Id: 1645345
• ClinVar RCV Id: RCV002148480
• dbSNP Id: rs781314311
• ExAC: 15:45003777 G / C
• gnomAD v2: 15-45003777-G-C
• gnomAD v3: 15-44711579-G-C
• gnomAD v4: 15-44711579-G-C
• MyVariant Identifiers: chr15:g.45003777G>C (hg19) ; chr15:g.44711579G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.44711579G>C , CM000677.2:g.44711579G>C	GRCh38
NC_000015.9:g.45003777G>C , CM000677.1:g.45003777G>C	GRCh37
NC_000015.8:g.42791069G>C	NCBI36
NG_012920.1:g.5093G>C
NG_012920.2:g.5103G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695792.1:n.83+139G>C
ENST00000648006.3:c.33G>C MANE Select	ENSP00000497910.1:p.Ala11=
ENST00000349264.10:c.33G>C	ENSP00000340858.6:p.Ala11=
ENST00000544417.5:c.33G>C	ENSP00000437604.2:p.Ala11=
ENST00000557901.5:c.33G>C	ENSP00000452861.1:p.Ala11=
ENST00000558401.5:c.33G>C	ENSP00000452780.1:p.Ala11=
ENST00000559720.5:n.93G>C
ENST00000559916.1:c.33G>C	ENSP00000453350.1:p.Ala11=
ENST00000561424.5:c.33G>C	ENSP00000453191.1:p.Ala11=
NM_004048.2:c.33G>C	NP_004039.1:p.Ala11=
XM_005254549.2:c.33G>C	XP_005254606.1:p.Ala11=
NM_004048.3:c.33G>C	NP_004039.1:p.Ala11=
XM_005254549.3:c.33G>C	XP_005254606.1:p.Ala11=
XR_002957658.1:n.88G>C
NM_004048.4:c.33G>C MANE Select	NP_004039.1:p.Ala11=