Canonical Allele Identifier: CA2702510582

Gene: MYD88

Linked Data

• dbSNP Id: rs2125780156

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.38141106C>T , CM000665.2:g.38141106C>T	GRCh38
NC_000003.11:g.38182597C>T , CM000665.1:g.38182597C>T	GRCh37
NC_000003.10:g.38157601C>T	NCBI36
NG_016964.1:g.7629C>T , LRG_157:g.7629C>T
NG_023225.1:g.1137G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000463956.2:n.524-26C>T
ENST00000484513.2:n.2215-26C>T
ENST00000699084.1:n.1826-26C>T
ENST00000699085.1:n.1602-26C>T
ENST00000699086.1:c.518-26C>T
ENST00000396334.8:c.737-26C>T	ENSP00000379625.4:n.737-26C>T
ENST00000416282.3:n.840-26C>T
ENST00000417037.8:c.602-26C>T	ENSP00000401399.4:n.602-26C>T
ENST00000421516.3:c.761-26C>T	ENSP00000391753.3:n.761-26C>T
ENST00000650112.2:c.421-26C>T	ENSP00000497991.2:n.421-26C>T
ENST00000650905.2:c.737-26C>T MANE Select	ENSP00000498360.2:n.737-26C>T
ENST00000651800.2:c.556-26C>T	ENSP00000499012.2:n.556-26C>T
ENST00000652213.1:c.718-26C>T	ENSP00000498576.1:n.718-26C>T
ENST00000652590.1:n.965-26C>T
ENST00000396334.7:c.776-26C>T	ENSP00000379625.3:n.776-26C>T
ENST00000416282.2:n.840-26C>T
ENST00000417037.6:c.800-26C>T	ENSP00000401399.2:n.800-26C>T
ENST00000421516.1:c.797-26C>T	ENSP00000391753.1:n.797-26C>T
ENST00000424893.5:c.641-26C>T	ENSP00000389979.1:n.641-26C>T
ENST00000443433.6:c.595-26C>T	ENSP00000390565.2:n.595-26C>T
ENST00000463956.1:n.450-26C>T
ENST00000481122.5:n.530-26C>T
ENST00000484513.1:n.1427-26C>T
ENST00000495303.5:c.460-26C>T	ENSP00000417848.1:n.460-26C>T
NM_001172566.1:c.460-26C>T	NP_001166037.1:n.460-26C>T
NM_001172567.1:c.800-26C>T , LRG_157t1:c.800-26C>T	NP_001166038.1:n.800-26C>T
NM_001172568.1:c.641-26C>T	NP_001166039.1:n.641-26C>T
NM_001172569.1:c.595-26C>T	NP_001166040.1:n.595-26C>T
NM_002468.4:c.776-26C>T	NP_002459.2:n.776-26C>T
XM_005265172.1:c.757-26C>T	XP_005265229.1:n.757-26C>T
XM_006713170.1:c.622-26C>T	XP_006713233.1:n.622-26C>T
NM_001172566.2:c.421-26C>T	NP_001166037.2:n.421-26C>T
NM_001172567.2:c.761-26C>T	NP_001166038.2:n.761-26C>T
NM_001172568.2:c.602-26C>T	NP_001166039.2:n.602-26C>T
NM_001172569.2:c.556-26C>T	NP_001166040.2:n.556-26C>T
NM_001365876.1:c.718-26C>T	NP_001352805.1:n.718-26C>T
NM_001365877.1:c.583-26C>T	NP_001352806.1:n.583-26C>T
NM_002468.5:c.737-26C>T MANE Select	NP_002459.3:n.737-26C>T
NM_001172569.3:c.556-26C>T	NP_001166040.2:n.556-26C>T
NM_001374787.1:c.694-26C>T	NP_001361716.1:n.694-26C>T
NM_001374788.1:c.269-26C>T	NP_001361717.1:n.269-26C>T
NR_164663.1:n.420-26C>T