Canonical Allele Identifier: CA372279802

Gene: MYC

Linked Data

• dbSNP Id: rs2130094062
• COSMIC: COSM4171769 ; COSM4171770
• MyVariant Identifiers: chr8:g.128750752C>G (hg19) ; chr8:g.127738506C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.127738506C>G , CM000670.2:g.127738506C>G	GRCh38
NC_000008.10:g.128750752C>G , CM000670.1:g.128750752C>G	GRCh37
NC_000008.9:g.128819934C>G	NCBI36
NG_007161.1:g.7437C>G
NG_007161.2:g.8073C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000707113.1:c.244C>G	ENSP00000516742.1:p.Leu82Val
ENST00000707114.1:c.244C>G	ENSP00000516743.1:p.Leu82Val
ENST00000707115.1:c.244C>G	ENSP00000516744.1:p.Leu82Val
ENST00000707116.1:c.244C>G	ENSP00000516745.1:p.Leu82Val
ENST00000517291.2:c.286C>G	ENSP00000429441.2:p.Leu96Val
ENST00000524013.2:c.286C>G	ENSP00000430235.2:p.Leu96Val
ENST00000621592.8:c.289C>G MANE Select	ENSP00000478887.2:p.Leu97Val
ENST00000651626.1:c.-57C>G	ENSP00000499182.1:n.-57C>G
ENST00000652288.1:c.244C>G	ENSP00000499105.1:p.Leu82Val
ENST00000259523.10:c.244C>G	ENSP00000259523.6:p.Leu82Val
ENST00000377970.6:c.244C>G	ENSP00000367207.3:p.Leu82Val
ENST00000517291.1:c.286C>G	ENSP00000429441.1:p.Leu96Val
ENST00000524013.1:c.286C>G	ENSP00000430235.1:p.Leu96Val
ENST00000613283.1:c.289C>G	ENSP00000479618.1:p.Leu97Val
ENST00000621592.5:c.289C>G	ENSP00000478887.1:p.Leu97Val
NM_002467.4:c.289C>G	NP_002458.2:p.Leu97Val
NM_001354870.1:c.286C>G	NP_001341799.1:p.Leu96Val
NM_002467.5:c.289C>G	NP_002458.2:p.Leu97Val
NM_002467.6:c.289C>G MANE Select	NP_002458.2:p.Leu97Val