Canonical Allele Identifier: CA72884382

Gene: MYD88

Linked Data

• dbSNP Id: rs137853064
• gnomAD v4: 3-38140510-C-A
• MyVariant Identifiers: chr3:g.38182001C>A (hg19) ; chr3:g.38140510C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.38140510C>A , CM000665.2:g.38140510C>A	GRCh38
NC_000003.11:g.38182001C>A , CM000665.1:g.38182001C>A	GRCh37
NC_000003.10:g.38157005C>A	NCBI36
NG_016964.1:g.7033C>A , LRG_157:g.7033C>A
NG_023225.1:g.1733G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000463956.2:n.373C>A
ENST00000484513.2:n.1876C>A
ENST00000699084.1:n.1487C>A
ENST00000699085.1:n.1451C>A
ENST00000699086.1:c.386C>A
ENST00000396334.8:c.586C>A	ENSP00000379625.4:p.Arg196Ser
ENST00000416282.3:n.501C>A
ENST00000417037.8:c.451C>A	ENSP00000401399.4:p.Arg151Ser
ENST00000421516.3:c.586C>A	ENSP00000391753.3:p.Arg196Ser
ENST00000650112.2:c.329-247C>A	ENSP00000497991.2:n.329-247C>A
ENST00000650905.2:c.586C>A MANE Select	ENSP00000498360.2:p.Arg196Ser
ENST00000651800.2:c.464-247C>A	ENSP00000499012.2:n.464-247C>A
ENST00000652213.1:c.586C>A	ENSP00000498576.1:p.Arg196Ser
ENST00000652590.1:n.626C>A
ENST00000396334.7:c.625C>A	ENSP00000379625.3:p.Arg209Ser
ENST00000416282.2:n.501C>A
ENST00000417037.6:c.625C>A	ENSP00000401399.2:p.Arg209Ser
ENST00000421516.1:c.622C>A	ENSP00000391753.1:p.Arg208Ser
ENST00000424893.5:c.490C>A	ENSP00000389979.1:p.Arg164Ser
ENST00000443433.6:c.503-247C>A	ENSP00000390565.2:n.503-247C>A
ENST00000460295.1:n.1019C>A
ENST00000463956.1:n.299C>A
ENST00000481122.5:n.379C>A
ENST00000484513.1:n.1088C>A
ENST00000495303.5:c.368-247C>A	ENSP00000417848.1:n.368-247C>A
NM_001172566.1:c.368-247C>A	NP_001166037.1:n.368-247C>A
NM_001172567.1:c.625C>A , LRG_157t1:c.625C>A	NP_001166038.1:p.Arg209Ser
NM_001172568.1:c.490C>A	NP_001166039.1:p.Arg164Ser
NM_001172569.1:c.503-247C>A	NP_001166040.1:n.503-247C>A
NM_002468.4:c.625C>A	NP_002459.2:p.Arg209Ser
XM_005265172.1:c.625C>A	XP_005265229.1:p.Arg209Ser
XM_006713170.1:c.490C>A	XP_006713233.1:p.Arg164Ser
NM_001172566.2:c.329-247C>A	NP_001166037.2:n.329-247C>A
NM_001172567.2:c.586C>A	NP_001166038.2:p.Arg196Ser
NM_001172568.2:c.451C>A	NP_001166039.2:p.Arg151Ser
NM_001172569.2:c.464-247C>A	NP_001166040.2:n.464-247C>A
NM_001365876.1:c.586C>A	NP_001352805.1:p.Arg196Ser
NM_001365877.1:c.451C>A	NP_001352806.1:p.Arg151Ser
NM_002468.5:c.586C>A MANE Select	NP_002459.3:p.Arg196Ser
NM_001172569.3:c.464-247C>A	NP_001166040.2:n.464-247C>A
NM_001374787.1:c.586C>A	NP_001361716.1:p.Arg196Ser
NM_001374788.1:c.118C>A	NP_001361717.1:p.Arg40Ser
NR_164663.1:n.288C>A