Canonical Allele Identifier: CA4875229
Gene: MYC HGNC NCBI

Linked Data

dbSNP Id: rs745993896

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.127738349G>A , CM000670.2:g.127738349G>A GRCh38
NC_000008.10:g.128750595G>A , CM000670.1:g.128750595G>A GRCh37
NC_000008.9:g.128819777G>A NCBI36
NG_007161.1:g.7280G>A
NG_007161.2:g.7916G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000707113.1:c.87G>A ENSP00000516742.1:p.Glu29=
ENST00000707114.1:c.87G>A ENSP00000516743.1:p.Glu29=
ENST00000707115.1:c.87G>A ENSP00000516744.1:p.Glu29=
ENST00000707116.1:c.87G>A ENSP00000516745.1:p.Glu29=
ENST00000517291.2:c.129G>A ENSP00000429441.2:p.Glu43=
ENST00000524013.2:c.129G>A ENSP00000430235.2:p.Glu43=
ENST00000621592.8:c.132G>A MANE Select ENSP00000478887.2:p.Glu44=
ENST00000651626.1:c.-214G>A ENSP00000499182.1:n.-214G>A
ENST00000652288.1:c.87G>A ENSP00000499105.1:p.Glu29=
ENST00000259523.10:c.87G>A ENSP00000259523.6:p.Glu29=
ENST00000377970.6:c.87G>A ENSP00000367207.3:p.Glu29=
ENST00000517291.1:c.129G>A ENSP00000429441.1:p.Glu43=
ENST00000520751.1:c.53G>A ENSP00000430226.1:p.Arg18Lys
ENST00000524013.1:c.129G>A ENSP00000430235.1:p.Glu43=
ENST00000613283.1:c.132G>A ENSP00000479618.1:p.Glu44=
ENST00000621592.5:c.132G>A ENSP00000478887.1:p.Glu44=
NM_002467.4:c.132G>A NP_002458.2:p.Glu44=
NM_001354870.1:c.129G>A NP_001341799.1:p.Glu43=
NM_002467.5:c.132G>A NP_002458.2:p.Glu44=
NM_002467.6:c.132G>A MANE Select NP_002458.2:p.Glu44=