Canonical Allele Identifier: CA4875237

Gene: MYC

Linked Data

• ClinVar Variation Id: 791168
• ClinVar RCV Id: RCV000974095
• dbSNP Id: rs61752959
• ExAC: 8:128750607 G / A
• gnomAD v2: 8-128750607-G-A
• gnomAD v3: 8-127738361-G-A
• gnomAD v4: 8-127738361-G-A
• MyVariant Identifiers: chr8:g.128750607G>A (hg19) ; chr8:g.127738361G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.127738361G>A , CM000670.2:g.127738361G>A	GRCh38
NC_000008.10:g.128750607G>A , CM000670.1:g.128750607G>A	GRCh37
NC_000008.9:g.128819789G>A	NCBI36
NG_007161.1:g.7292G>A
NG_007161.2:g.7928G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000707113.1:c.99G>A	ENSP00000516742.1:p.Gln33=
ENST00000707114.1:c.99G>A	ENSP00000516743.1:p.Gln33=
ENST00000707115.1:c.99G>A	ENSP00000516744.1:p.Gln33=
ENST00000707116.1:c.99G>A	ENSP00000516745.1:p.Gln33=
ENST00000517291.2:c.141G>A	ENSP00000429441.2:p.Gln47=
ENST00000524013.2:c.141G>A	ENSP00000430235.2:p.Gln47=
ENST00000621592.8:c.144G>A MANE Select	ENSP00000478887.2:p.Gln48=
ENST00000651626.1:c.-202G>A	ENSP00000499182.1:n.-202G>A
ENST00000652288.1:c.99G>A	ENSP00000499105.1:p.Gln33=
ENST00000259523.10:c.99G>A	ENSP00000259523.6:p.Gln33=
ENST00000377970.6:c.99G>A	ENSP00000367207.3:p.Gln33=
ENST00000517291.1:c.141G>A	ENSP00000429441.1:p.Gln47=
ENST00000520751.1:c.65G>A	ENSP00000430226.1:p.Ser22Asn
ENST00000524013.1:c.141G>A	ENSP00000430235.1:p.Gln47=
ENST00000613283.1:c.144G>A	ENSP00000479618.1:p.Gln48=
ENST00000621592.5:c.144G>A	ENSP00000478887.1:p.Gln48=
NM_002467.4:c.144G>A	NP_002458.2:p.Gln48=
NM_001354870.1:c.141G>A	NP_001341799.1:p.Gln47=
NM_002467.5:c.144G>A	NP_002458.2:p.Gln48=
NM_002467.6:c.144G>A MANE Select	NP_002458.2:p.Gln48=