Canonical Allele Identifier: CA11567783

Gene: MYD88

Linked Data

• dbSNP Id: rs6853
• gnomAD v2: 3-38184370-A-G
• gnomAD v3: 3-38142879-A-G
• gnomAD v4: 3-38142879-A-G
• MyVariant Identifiers: chr3:g.38184370A>G (hg19) ; chr3:g.38142879A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.38142879A>G , CM000665.2:g.38142879A>G	GRCh38
NC_000003.11:g.38184370A>G , CM000665.1:g.38184370A>G	GRCh37
NC_000003.10:g.38159374A>G	NCBI36
NG_016964.1:g.9402A>G , LRG_157:g.9402A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000463956.2:n.2271A>G
ENST00000484513.2:n.3962A>G
ENST00000699084.1:n.3573A>G
ENST00000699085.1:n.3349A>G
ENST00000699086.1:c.2265A>G
ENST00000396334.8:c.*1593A>G	ENSP00000379625.4:n.*1593A>G
ENST00000416282.3:n.2587A>G
ENST00000417037.8:c.*1593A>G	ENSP00000401399.4:n.*1593A>G
ENST00000421516.3:c.*1593A>G	ENSP00000391753.3:n.*1593A>G
ENST00000650112.2:c.*1727A>G	ENSP00000497991.2:n.*1727A>G
ENST00000650905.2:c.*1593A>G MANE Select	ENSP00000498360.2:n.*1593A>G
ENST00000651800.2:c.*1727A>G	ENSP00000499012.2:n.*1727A>G
ENST00000652213.1:c.*1727A>G	ENSP00000498576.1:n.*1727A>G
ENST00000652590.1:n.2712A>G
ENST00000396334.7:c.*1593A>G	ENSP00000379625.3:n.*1593A>G
ENST00000416282.2:n.2587A>G
ENST00000417037.6:c.*1593A>G	ENSP00000401399.2:n.*1593A>G
ENST00000421516.1:c.2544A>G	ENSP00000391753.1:n.2544A>G
ENST00000484513.1:n.3174A>G
NM_001172566.1:c.*1727A>G	NP_001166037.1:n.*1727A>G
NM_001172567.1:c.*1593A>G , LRG_157t1:c.*1593A>G	NP_001166038.1:n.*1593A>G
NM_001172568.1:c.*1593A>G	NP_001166039.1:n.*1593A>G
NM_001172569.1:c.*1727A>G	NP_001166040.1:n.*1727A>G
NM_002468.4:c.*1593A>G	NP_002459.2:n.*1593A>G
XM_005265172.1:c.*1727A>G	XP_005265229.1:n.*1727A>G
XM_006713170.1:c.*1727A>G	XP_006713233.1:n.*1727A>G
NM_001172566.2:c.*1727A>G	NP_001166037.2:n.*1727A>G
NM_001172567.2:c.*1593A>G	NP_001166038.2:n.*1593A>G
NM_001172568.2:c.*1593A>G	NP_001166039.2:n.*1593A>G
NM_001172569.2:c.*1727A>G	NP_001166040.2:n.*1727A>G
NM_001365876.1:c.*1727A>G	NP_001352805.1:n.*1727A>G
NM_001365877.1:c.*1727A>G	NP_001352806.1:n.*1727A>G
NM_002468.5:c.*1593A>G MANE Select	NP_002459.3:n.*1593A>G
NM_001172569.3:c.*1727A>G	NP_001166040.2:n.*1727A>G
NM_001374787.1:c.*1727A>G	NP_001361716.1:n.*1727A>G
NM_001374788.1:c.*1593A>G	NP_001361717.1:n.*1593A>G
NR_164663.1:n.2167A>G