Canonical Allele Identifier: CA392232239

Gene: B2M

Linked Data

• dbSNP Id: rs757230673
• MyVariant Identifiers: chr15:g.45003805A>T (hg19) ; chr15:g.44711607A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.44711607A>T , CM000677.2:g.44711607A>T	GRCh38
NC_000015.9:g.45003805A>T , CM000677.1:g.45003805A>T	GRCh37
NC_000015.8:g.42791097A>T	NCBI36
NG_012920.1:g.5121A>T
NG_012920.2:g.5131A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695792.1:n.83+167A>T
ENST00000648006.3:c.61A>T MANE Select	ENSP00000497910.1:p.Ile21Phe
ENST00000349264.10:c.57+4A>T	ENSP00000340858.6:n.57+4A>T
ENST00000544417.5:c.61A>T	ENSP00000437604.2:p.Ile21Phe
ENST00000557901.5:c.61A>T	ENSP00000452861.1:p.Ile21Phe
ENST00000558401.5:c.61A>T	ENSP00000452780.1:p.Ile21Phe
ENST00000559720.5:n.121A>T
ENST00000559916.1:c.61A>T	ENSP00000453350.1:p.Ile21Phe
ENST00000561424.5:c.61A>T	ENSP00000453191.1:p.Ile21Phe
NM_004048.2:c.61A>T	NP_004039.1:p.Ile21Phe
XM_005254549.2:c.61A>T	XP_005254606.1:p.Ile21Phe
NM_004048.3:c.61A>T	NP_004039.1:p.Ile21Phe
XM_005254549.3:c.61A>T	XP_005254606.1:p.Ile21Phe
XR_002957658.1:n.116A>T
NM_004048.4:c.61A>T MANE Select	NP_004039.1:p.Ile21Phe