Canonical Allele Identifier: CA2316226

Gene: MYD88

Linked Data

• dbSNP Id: rs777953448
• ExAC: 3:38182645 C / A
• gnomAD v2: 3-38182645-C-A
• gnomAD v4: 3-38141154-C-A
• MyVariant Identifiers: chr3:g.38182645C>A (hg19) ; chr3:g.38141154C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.38141154C>A , CM000665.2:g.38141154C>A	GRCh38
NC_000003.11:g.38182645C>A , CM000665.1:g.38182645C>A	GRCh37
NC_000003.10:g.38157649C>A	NCBI36
NG_016964.1:g.7677C>A , LRG_157:g.7677C>A
NG_023225.1:g.1089G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000463956.2:n.546C>A
ENST00000484513.2:n.2237C>A
ENST00000699084.1:n.1848C>A
ENST00000699085.1:n.1624C>A
ENST00000699086.1:c.540C>A
ENST00000396334.8:c.759C>A	ENSP00000379625.4:p.Ile253=
ENST00000416282.3:n.862C>A
ENST00000417037.8:c.624C>A	ENSP00000401399.4:p.Ile208=
ENST00000421516.3:c.783C>A	ENSP00000391753.3:p.Ile261=
ENST00000650112.2:c.*2C>A	ENSP00000497991.2:n.*2C>A
ENST00000650905.2:c.759C>A MANE Select	ENSP00000498360.2:p.Ile253=
ENST00000651800.2:c.*2C>A	ENSP00000499012.2:n.*2C>A
ENST00000652213.1:c.*2C>A	ENSP00000498576.1:n.*2C>A
ENST00000652590.1:n.987C>A
ENST00000396334.7:c.798C>A	ENSP00000379625.3:p.Ile266=
ENST00000416282.2:n.862C>A
ENST00000417037.6:c.822C>A	ENSP00000401399.2:p.Ile274=
ENST00000421516.1:c.819C>A	ENSP00000391753.1:p.Ile273=
ENST00000424893.5:c.663C>A	ENSP00000389979.1:p.Ile221=
ENST00000443433.6:c.*2C>A	ENSP00000390565.2:n.*2C>A
ENST00000463956.1:n.472C>A
ENST00000481122.5:n.552C>A
ENST00000484513.1:n.1449C>A
ENST00000495303.5:c.*2C>A	ENSP00000417848.1:n.*2C>A
NM_001172566.1:c.*2C>A	NP_001166037.1:n.*2C>A
NM_001172567.1:c.822C>A , LRG_157t1:c.822C>A	NP_001166038.1:p.Ile274=
NM_001172568.1:c.663C>A	NP_001166039.1:p.Ile221=
NM_001172569.1:c.*2C>A	NP_001166040.1:n.*2C>A
NM_002468.4:c.798C>A	NP_002459.2:p.Ile266=
XM_005265172.1:c.*2C>A	XP_005265229.1:n.*2C>A
XM_006713170.1:c.*2C>A	XP_006713233.1:n.*2C>A
NM_001172566.2:c.*2C>A	NP_001166037.2:n.*2C>A
NM_001172567.2:c.783C>A	NP_001166038.2:p.Ile261=
NM_001172568.2:c.624C>A	NP_001166039.2:p.Ile208=
NM_001172569.2:c.*2C>A	NP_001166040.2:n.*2C>A
NM_001365876.1:c.*2C>A	NP_001352805.1:n.*2C>A
NM_001365877.1:c.*2C>A	NP_001352806.1:n.*2C>A
NM_002468.5:c.759C>A MANE Select	NP_002459.3:p.Ile253=
NM_001172569.3:c.*2C>A	NP_001166040.2:n.*2C>A
NM_001374787.1:c.*2C>A	NP_001361716.1:n.*2C>A
NM_001374788.1:c.291C>A	NP_001361717.1:p.Ile97=
NR_164663.1:n.442C>A