Canonical Allele Identifier: CA462988142
Gene: MYC HGNC NCBI

Linked Data

dbSNP Id: rs1264182362
MyVariant Identifiers: chr8:g.128750778C>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.127738532C>A , CM000670.2:g.127738532C>A GRCh38
NC_000008.10:g.128750778C>A , CM000670.1:g.128750778C>A GRCh37
NC_000008.9:g.128819960C>A NCBI36
NG_007161.1:g.7463C>A
NG_007161.2:g.8099C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000707113.1:c.270C>A ENSP00000516742.1:p.Gly90=
ENST00000707114.1:c.270C>A ENSP00000516743.1:p.Gly90=
ENST00000707115.1:c.270C>A ENSP00000516744.1:p.Gly90=
ENST00000707116.1:c.270C>A ENSP00000516745.1:p.Gly90=
ENST00000517291.2:c.312C>A ENSP00000429441.2:p.Gly104=
ENST00000524013.2:c.312C>A ENSP00000430235.2:p.Gly104=
ENST00000621592.8:c.315C>A MANE Select ENSP00000478887.2:p.Gly105=
ENST00000651626.1:c.-31C>A ENSP00000499182.1:n.-31C>A
ENST00000652288.1:c.270C>A ENSP00000499105.1:p.Gly90=
ENST00000259523.10:c.270C>A ENSP00000259523.6:p.Gly90=
ENST00000377970.6:c.270C>A ENSP00000367207.3:p.Gly90=
ENST00000517291.1:c.312C>A ENSP00000429441.1:p.Gly104=
ENST00000524013.1:c.312C>A ENSP00000430235.1:p.Gly104=
ENST00000613283.1:c.315C>A ENSP00000479618.1:p.Gly105=
ENST00000621592.5:c.315C>A ENSP00000478887.1:p.Gly105=
NM_002467.4:c.315C>A NP_002458.2:p.Gly105=
NM_001354870.1:c.312C>A NP_001341799.1:p.Gly104=
NM_002467.5:c.315C>A NP_002458.2:p.Gly105=
NM_002467.6:c.315C>A MANE Select NP_002458.2:p.Gly105=