Canonical Allele Identifier: CA270116941
Gene: B2M HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.44715421A>G , CM000677.2:g.44715421A>G GRCh38
NC_000015.9:g.45007619A>G , CM000677.1:g.45007619A>G GRCh37
NC_000015.8:g.42794911A>G NCBI36
NG_012920.1:g.8935A>G
NG_012920.2:g.8945A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000695792.1:n.84-2A>G
ENST00000648006.3:c.68-2A>G MANE Select ENSP00000497910.1:n.68-2A>G
ENST00000349264.10:c.58-125A>G ENSP00000340858.6:n.58-125A>G
ENST00000544417.5:c.68-2A>G ENSP00000437604.2:n.68-2A>G
ENST00000557901.5:c.68-13A>G ENSP00000452861.1:n.68-13A>G
ENST00000558401.5:c.68-2A>G ENSP00000452780.1:n.68-2A>G
ENST00000559220.1:n.42+873A>G
ENST00000559720.5:n.128-2A>G
ENST00000559907.5:n.95-2A>G
ENST00000559916.1:c.68-2A>G ENSP00000453350.1:n.68-2A>G
ENST00000560681.1:n.63-2A>G
ENST00000561424.5:c.68-2A>G ENSP00000453191.1:n.68-2A>G
NM_004048.2:c.68-2A>G NP_004039.1:n.68-2A>G
XM_005254549.2:c.68-2A>G XP_005254606.1:n.68-2A>G
NM_004048.3:c.68-2A>G NP_004039.1:n.68-2A>G
XM_005254549.3:c.68-2A>G XP_005254606.1:n.68-2A>G
XR_002957658.1:n.123-2A>G
NM_004048.4:c.68-2A>G MANE Select NP_004039.1:n.68-2A>G
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