Canonical Allele Identifier: CA2316217

Gene: MYD88

Linked Data

• dbSNP Id: rs761665622
• ExAC: 3:38182591 C / G
• gnomAD v2: 3-38182591-C-G
• gnomAD v4: 3-38141100-C-G
• MyVariant Identifiers: chr3:g.38182591C>G (hg19) ; chr3:g.38141100C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.38141100C>G , CM000665.2:g.38141100C>G	GRCh38
NC_000003.11:g.38182591C>G , CM000665.1:g.38182591C>G	GRCh37
NC_000003.10:g.38157595C>G	NCBI36
NG_016964.1:g.7623C>G , LRG_157:g.7623C>G
NG_023225.1:g.1143G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000463956.2:n.524-32C>G
ENST00000484513.2:n.2215-32C>G
ENST00000699084.1:n.1826-32C>G
ENST00000699085.1:n.1602-32C>G
ENST00000699086.1:c.518-32C>G
ENST00000396334.8:c.737-32C>G	ENSP00000379625.4:n.737-32C>G
ENST00000416282.3:n.840-32C>G
ENST00000417037.8:c.602-32C>G	ENSP00000401399.4:n.602-32C>G
ENST00000421516.3:c.761-32C>G	ENSP00000391753.3:n.761-32C>G
ENST00000650112.2:c.421-32C>G	ENSP00000497991.2:n.421-32C>G
ENST00000650905.2:c.737-32C>G MANE Select	ENSP00000498360.2:n.737-32C>G
ENST00000651800.2:c.556-32C>G	ENSP00000499012.2:n.556-32C>G
ENST00000652213.1:c.718-32C>G	ENSP00000498576.1:n.718-32C>G
ENST00000652590.1:n.965-32C>G
ENST00000396334.7:c.776-32C>G	ENSP00000379625.3:n.776-32C>G
ENST00000416282.2:n.840-32C>G
ENST00000417037.6:c.800-32C>G	ENSP00000401399.2:n.800-32C>G
ENST00000421516.1:c.797-32C>G	ENSP00000391753.1:n.797-32C>G
ENST00000424893.5:c.641-32C>G	ENSP00000389979.1:n.641-32C>G
ENST00000443433.6:c.595-32C>G	ENSP00000390565.2:n.595-32C>G
ENST00000463956.1:n.450-32C>G
ENST00000481122.5:n.530-32C>G
ENST00000484513.1:n.1427-32C>G
ENST00000495303.5:c.460-32C>G	ENSP00000417848.1:n.460-32C>G
NM_001172566.1:c.460-32C>G	NP_001166037.1:n.460-32C>G
NM_001172567.1:c.800-32C>G , LRG_157t1:c.800-32C>G	NP_001166038.1:n.800-32C>G
NM_001172568.1:c.641-32C>G	NP_001166039.1:n.641-32C>G
NM_001172569.1:c.595-32C>G	NP_001166040.1:n.595-32C>G
NM_002468.4:c.776-32C>G	NP_002459.2:n.776-32C>G
XM_005265172.1:c.757-32C>G	XP_005265229.1:n.757-32C>G
XM_006713170.1:c.622-32C>G	XP_006713233.1:n.622-32C>G
NM_001172566.2:c.421-32C>G	NP_001166037.2:n.421-32C>G
NM_001172567.2:c.761-32C>G	NP_001166038.2:n.761-32C>G
NM_001172568.2:c.602-32C>G	NP_001166039.2:n.602-32C>G
NM_001172569.2:c.556-32C>G	NP_001166040.2:n.556-32C>G
NM_001365876.1:c.718-32C>G	NP_001352805.1:n.718-32C>G
NM_001365877.1:c.583-32C>G	NP_001352806.1:n.583-32C>G
NM_002468.5:c.737-32C>G MANE Select	NP_002459.3:n.737-32C>G
NM_001172569.3:c.556-32C>G	NP_001166040.2:n.556-32C>G
NM_001374787.1:c.694-32C>G	NP_001361716.1:n.694-32C>G
NM_001374788.1:c.269-32C>G	NP_001361717.1:n.269-32C>G
NR_164663.1:n.420-32C>G