Canonical Allele Identifier: CA490206928

Gene: B2M

Linked Data

• dbSNP Id: rs1341857550
• gnomAD v2: 15-45003786-T-C
• gnomAD v4: 15-44711588-T-C
• MyVariant Identifiers: chr15:g.45003786T>C (hg19) ; chr15:g.44711588T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.44711588T>C , CM000677.2:g.44711588T>C	GRCh38
NC_000015.9:g.45003786T>C , CM000677.1:g.45003786T>C	GRCh37
NC_000015.8:g.42791078T>C	NCBI36
NG_012920.1:g.5102T>C
NG_012920.2:g.5112T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695792.1:n.83+148T>C
ENST00000648006.3:c.42T>C MANE Select	ENSP00000497910.1:p.Ser14=
ENST00000349264.10:c.42T>C	ENSP00000340858.6:p.Ser14=
ENST00000544417.5:c.42T>C	ENSP00000437604.2:p.Ser14=
ENST00000557901.5:c.42T>C	ENSP00000452861.1:p.Ser14=
ENST00000558401.5:c.42T>C	ENSP00000452780.1:p.Ser14=
ENST00000559720.5:n.102T>C
ENST00000559916.1:c.42T>C	ENSP00000453350.1:p.Ser14=
ENST00000561424.5:c.42T>C	ENSP00000453191.1:p.Ser14=
NM_004048.2:c.42T>C	NP_004039.1:p.Ser14=
XM_005254549.2:c.42T>C	XP_005254606.1:p.Ser14=
NM_004048.3:c.42T>C	NP_004039.1:p.Ser14=
XM_005254549.3:c.42T>C	XP_005254606.1:p.Ser14=
XR_002957658.1:n.97T>C
NM_004048.4:c.42T>C MANE Select	NP_004039.1:p.Ser14=