Canonical Allele Identifier: CA4875218

Gene: MYC

Linked Data

• dbSNP Id: rs146505192
• ExAC: 8:128750527 T / G
• gnomAD v2: 8-128750527-T-G
• gnomAD v4: 8-127738281-T-G
• MyVariant Identifiers: chr8:g.128750527T>G (hg19) ; chr8:g.127738281T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.127738281T>G , CM000670.2:g.127738281T>G	GRCh38
NC_000008.10:g.128750527T>G , CM000670.1:g.128750527T>G	GRCh37
NC_000008.9:g.128819709T>G	NCBI36
NG_007161.1:g.7212T>G
NG_007161.2:g.7848T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000707113.1:c.19T>G	ENSP00000516742.1:p.Phe7Val
ENST00000707114.1:c.19T>G	ENSP00000516743.1:p.Phe7Val
ENST00000707115.1:c.19T>G	ENSP00000516744.1:p.Phe7Val
ENST00000707116.1:c.19T>G	ENSP00000516745.1:p.Phe7Val
ENST00000517291.2:c.61T>G	ENSP00000429441.2:p.Phe21Val
ENST00000524013.2:c.61T>G	ENSP00000430235.2:p.Phe21Val
ENST00000621592.8:c.64T>G MANE Select	ENSP00000478887.2:p.Phe22Val
ENST00000651626.1:c.-282T>G	ENSP00000499182.1:n.-282T>G
ENST00000652288.1:c.19T>G	ENSP00000499105.1:p.Phe7Val
ENST00000259523.10:c.19T>G	ENSP00000259523.6:p.Phe7Val
ENST00000377970.6:c.19T>G	ENSP00000367207.3:p.Phe7Val
ENST00000517291.1:c.61T>G	ENSP00000429441.1:p.Phe21Val
ENST00000520751.1:c.-5-11T>G	ENSP00000430226.1:n.-5-11T>G
ENST00000524013.1:c.61T>G	ENSP00000430235.1:p.Phe21Val
ENST00000613283.1:c.64T>G	ENSP00000479618.1:p.Phe22Val
ENST00000621592.5:c.64T>G	ENSP00000478887.1:p.Phe22Val
NM_002467.4:c.64T>G	NP_002458.2:p.Phe22Val
NM_001354870.1:c.61T>G	NP_001341799.1:p.Phe21Val
NM_002467.5:c.64T>G	NP_002458.2:p.Phe22Val
NM_002467.6:c.64T>G MANE Select	NP_002458.2:p.Phe22Val