Canonical Allele Identifier: CA433330212

Gene: MYD88

Linked Data

• dbSNP Id: rs2125778746
• gnomAD v4: 3-38140519-C-T
• MyVariant Identifiers: chr3:g.38182010C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.38140519C>T , CM000665.2:g.38140519C>T	GRCh38
NC_000003.11:g.38182010C>T , CM000665.1:g.38182010C>T	GRCh37
NC_000003.10:g.38157014C>T	NCBI36
NG_016964.1:g.7042C>T , LRG_157:g.7042C>T
NG_023225.1:g.1724G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000463956.2:n.382C>T
ENST00000484513.2:n.1885C>T
ENST00000699084.1:n.1496C>T
ENST00000699085.1:n.1460C>T
ENST00000699086.1:c.395C>T
ENST00000396334.8:c.595C>T	ENSP00000379625.4:p.Leu199=
ENST00000416282.3:n.510C>T
ENST00000417037.8:c.460C>T	ENSP00000401399.4:p.Leu154=
ENST00000421516.3:c.595C>T	ENSP00000391753.3:p.Leu199=
ENST00000650112.2:c.329-238C>T	ENSP00000497991.2:n.329-238C>T
ENST00000650905.2:c.595C>T MANE Select	ENSP00000498360.2:p.Leu199=
ENST00000651800.2:c.464-238C>T	ENSP00000499012.2:n.464-238C>T
ENST00000652213.1:c.595C>T	ENSP00000498576.1:p.Leu199=
ENST00000652590.1:n.635C>T
ENST00000396334.7:c.634C>T	ENSP00000379625.3:p.Leu212=
ENST00000416282.2:n.510C>T
ENST00000417037.6:c.634C>T	ENSP00000401399.2:p.Leu212=
ENST00000421516.1:c.631C>T	ENSP00000391753.1:p.Leu211=
ENST00000424893.5:c.499C>T	ENSP00000389979.1:p.Leu167=
ENST00000443433.6:c.503-238C>T	ENSP00000390565.2:n.503-238C>T
ENST00000460295.1:n.1028C>T
ENST00000463956.1:n.308C>T
ENST00000481122.5:n.388C>T
ENST00000484513.1:n.1097C>T
ENST00000495303.5:c.368-238C>T	ENSP00000417848.1:n.368-238C>T
NM_001172566.1:c.368-238C>T	NP_001166037.1:n.368-238C>T
NM_001172567.1:c.634C>T , LRG_157t1:c.634C>T	NP_001166038.1:p.Leu212=
NM_001172568.1:c.499C>T	NP_001166039.1:p.Leu167=
NM_001172569.1:c.503-238C>T	NP_001166040.1:n.503-238C>T
NM_002468.4:c.634C>T	NP_002459.2:p.Leu212=
XM_005265172.1:c.634C>T	XP_005265229.1:p.Leu212=
XM_006713170.1:c.499C>T	XP_006713233.1:p.Leu167=
NM_001172566.2:c.329-238C>T	NP_001166037.2:n.329-238C>T
NM_001172567.2:c.595C>T	NP_001166038.2:p.Leu199=
NM_001172568.2:c.460C>T	NP_001166039.2:p.Leu154=
NM_001172569.2:c.464-238C>T	NP_001166040.2:n.464-238C>T
NM_001365876.1:c.595C>T	NP_001352805.1:p.Leu199=
NM_001365877.1:c.460C>T	NP_001352806.1:p.Leu154=
NM_002468.5:c.595C>T MANE Select	NP_002459.3:p.Leu199=
NM_001172569.3:c.464-238C>T	NP_001166040.2:n.464-238C>T
NM_001374787.1:c.595C>T	NP_001361716.1:p.Leu199=
NM_001374788.1:c.127C>T	NP_001361717.1:p.Leu43=
NR_164663.1:n.297C>T