Canonical Allele Identifier: CA2628214549

Gene: B2M

Linked Data

• gnomAD v4: 15-44711713-A-AGGAGAACTTGGAGAAG

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.44711714_44711715insGAGAACTTGGAGAAGG , CM000677.2:g.44711714_44711715insGAGAACTTGGAGAAGG	GRCh38
NC_000015.9:g.45003912_45003913insGAGAACTTGGAGAAGG , CM000677.1:g.45003912_45003913insGAGAACTTGGAGAAGG	GRCh37
NC_000015.8:g.42791204_42791205insGAGAACTTGGAGAAGG	NCBI36
NG_012920.1:g.5228_5229insGAGAACTTGGAGAAGG
NG_012920.2:g.5238_5239insGAGAACTTGGAGAAGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695792.1:n.83+274_83+275insGAGAACTTGGAGAAGG
ENST00000648006.3:c.67+101_67+102insGAGAACTTGGAGAAGG MANE Select	ENSP00000497910.1:n.67+101_67+102insGAGAACTTGGAGAAGG
ENST00000349264.10:c.57+111_57+112insGAGAACTTGGAGAAGG	ENSP00000340858.6:n.57+111_57+112insGAGAACTTGGAGAAGG
ENST00000544417.5:c.67+101_67+102insGAGAACTTGGAGAAGG	ENSP00000437604.2:n.67+101_67+102insGAGAACTTGGAGAAGG
ENST00000557901.5:c.67+101_67+102insGAGAACTTGGAGAAGG	ENSP00000452861.1:n.67+101_67+102insGAGAACTTGGAGAAGG
ENST00000558401.5:c.67+101_67+102insGAGAACTTGGAGAAGG	ENSP00000452780.1:n.67+101_67+102insGAGAACTTGGAGAAGG
ENST00000559720.5:n.127+101_127+102insGAGAACTTGGAGAAGG
ENST00000559916.1:c.67+101_67+102insGAGAACTTGGAGAAGG	ENSP00000453350.1:n.67+101_67+102insGAGAACTTGGAGAAGG
ENST00000561424.5:c.67+101_67+102insGAGAACTTGGAGAAGG	ENSP00000453191.1:n.67+101_67+102insGAGAACTTGGAGAAGG
NM_004048.2:c.67+101_67+102insGAGAACTTGGAGAAGG	NP_004039.1:n.67+101_67+102insGAGAACTTGGAGAAGG
XM_005254549.2:c.67+101_67+102insGAGAACTTGGAGAAGG	XP_005254606.1:n.67+101_67+102insGAGAACTTGGAGAAGG
NM_004048.3:c.67+101_67+102insGAGAACTTGGAGAAGG	NP_004039.1:n.67+101_67+102insGAGAACTTGGAGAAGG
XM_005254549.3:c.67+101_67+102insGAGAACTTGGAGAAGG	XP_005254606.1:n.67+101_67+102insGAGAACTTGGAGAAGG
XR_002957658.1:n.122+101_122+102insGAGAACTTGGAGAAGG
NM_004048.4:c.67+101_67+102insGAGAACTTGGAGAAGG MANE Select	NP_004039.1:n.67+101_67+102insGAGAACTTGGAGAAGG