Canonical Allele Identifier: CA2316165

Gene: MYD88

Linked Data

• dbSNP Id: rs551708165
• ExAC: 3:38182006 T / C
• gnomAD v2: 3-38182006-T-C
• gnomAD v3: 3-38140515-T-C
• gnomAD v4: 3-38140515-T-C
• MyVariant Identifiers: chr3:g.38182006T>C (hg19) ; chr3:g.38140515T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.38140515T>C , CM000665.2:g.38140515T>C	GRCh38
NC_000003.11:g.38182006T>C , CM000665.1:g.38182006T>C	GRCh37
NC_000003.10:g.38157010T>C	NCBI36
NG_016964.1:g.7038T>C , LRG_157:g.7038T>C
NG_023225.1:g.1728A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000463956.2:n.378T>C
ENST00000484513.2:n.1881T>C
ENST00000699084.1:n.1492T>C
ENST00000699085.1:n.1456T>C
ENST00000699086.1:c.391T>C
ENST00000396334.8:c.591T>C	ENSP00000379625.4:p.Asp197=
ENST00000416282.3:n.506T>C
ENST00000417037.8:c.456T>C	ENSP00000401399.4:p.Asp152=
ENST00000421516.3:c.591T>C	ENSP00000391753.3:p.Asp197=
ENST00000650112.2:c.329-242T>C	ENSP00000497991.2:n.329-242T>C
ENST00000650905.2:c.591T>C MANE Select	ENSP00000498360.2:p.Asp197=
ENST00000651800.2:c.464-242T>C	ENSP00000499012.2:n.464-242T>C
ENST00000652213.1:c.591T>C	ENSP00000498576.1:p.Asp197=
ENST00000652590.1:n.631T>C
ENST00000396334.7:c.630T>C	ENSP00000379625.3:p.Asp210=
ENST00000416282.2:n.506T>C
ENST00000417037.6:c.630T>C	ENSP00000401399.2:p.Asp210=
ENST00000421516.1:c.627T>C	ENSP00000391753.1:p.Asp209=
ENST00000424893.5:c.495T>C	ENSP00000389979.1:p.Asp165=
ENST00000443433.6:c.503-242T>C	ENSP00000390565.2:n.503-242T>C
ENST00000460295.1:n.1024T>C
ENST00000463956.1:n.304T>C
ENST00000481122.5:n.384T>C
ENST00000484513.1:n.1093T>C
ENST00000495303.5:c.368-242T>C	ENSP00000417848.1:n.368-242T>C
NM_001172566.1:c.368-242T>C	NP_001166037.1:n.368-242T>C
NM_001172567.1:c.630T>C , LRG_157t1:c.630T>C	NP_001166038.1:p.Asp210=
NM_001172568.1:c.495T>C	NP_001166039.1:p.Asp165=
NM_001172569.1:c.503-242T>C	NP_001166040.1:n.503-242T>C
NM_002468.4:c.630T>C	NP_002459.2:p.Asp210=
XM_005265172.1:c.630T>C	XP_005265229.1:p.Asp210=
XM_006713170.1:c.495T>C	XP_006713233.1:p.Asp165=
NM_001172566.2:c.329-242T>C	NP_001166037.2:n.329-242T>C
NM_001172567.2:c.591T>C	NP_001166038.2:p.Asp197=
NM_001172568.2:c.456T>C	NP_001166039.2:p.Asp152=
NM_001172569.2:c.464-242T>C	NP_001166040.2:n.464-242T>C
NM_001365876.1:c.591T>C	NP_001352805.1:p.Asp197=
NM_001365877.1:c.456T>C	NP_001352806.1:p.Asp152=
NM_002468.5:c.591T>C MANE Select	NP_002459.3:p.Asp197=
NM_001172569.3:c.464-242T>C	NP_001166040.2:n.464-242T>C
NM_001374787.1:c.591T>C	NP_001361716.1:p.Asp197=
NM_001374788.1:c.123T>C	NP_001361717.1:p.Asp41=
NR_164663.1:n.293T>C