Canonical Allele Identifier: CA372279781
Gene: MYC HGNC NCBI

Linked Data

dbSNP Id: rs2130093997

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.127738497C>A , CM000670.2:g.127738497C>A GRCh38
NC_000008.10:g.128750743C>A , CM000670.1:g.128750743C>A GRCh37
NC_000008.9:g.128819925C>A NCBI36
NG_007161.1:g.7428C>A
NG_007161.2:g.8064C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000707113.1:c.235C>A ENSP00000516742.1:p.Pro79Thr
ENST00000707114.1:c.235C>A ENSP00000516743.1:p.Pro79Thr
ENST00000707115.1:c.235C>A ENSP00000516744.1:p.Pro79Thr
ENST00000707116.1:c.235C>A ENSP00000516745.1:p.Pro79Thr
ENST00000517291.2:c.277C>A ENSP00000429441.2:p.Pro93Thr
ENST00000524013.2:c.277C>A ENSP00000430235.2:p.Pro93Thr
ENST00000621592.8:c.280C>A MANE Select ENSP00000478887.2:p.Pro94Thr
ENST00000651626.1:c.-66C>A ENSP00000499182.1:n.-66C>A
ENST00000652288.1:c.235C>A ENSP00000499105.1:p.Pro79Thr
ENST00000259523.10:c.235C>A ENSP00000259523.6:p.Pro79Thr
ENST00000377970.6:c.235C>A ENSP00000367207.3:p.Pro79Thr
ENST00000517291.1:c.277C>A ENSP00000429441.1:p.Pro93Thr
ENST00000524013.1:c.277C>A ENSP00000430235.1:p.Pro93Thr
ENST00000613283.1:c.280C>A ENSP00000479618.1:p.Pro94Thr
ENST00000621592.5:c.280C>A ENSP00000478887.1:p.Pro94Thr
NM_002467.4:c.280C>A NP_002458.2:p.Pro94Thr
NM_001354870.1:c.277C>A NP_001341799.1:p.Pro93Thr
NM_002467.5:c.280C>A NP_002458.2:p.Pro94Thr
NM_002467.6:c.280C>A MANE Select NP_002458.2:p.Pro94Thr