Canonical Allele Identifier: CA4875220

Gene: MYC

Linked Data

• ClinVar Variation Id: 1679939
• ClinVar RCV Id: RCV002227948 ; RCV003971198
• dbSNP Id: rs4645959
• ExAC: 8:128750540 A / G
• gnomAD v2: 8-128750540-A-G
• gnomAD v3: 8-127738294-A-G
• gnomAD v4: 8-127738294-A-G
• MyVariant Identifiers: chr8:g.128750540A>G (hg19) ; chr8:g.127738294A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.127738294A>G , CM000670.2:g.127738294A>G	GRCh38
NC_000008.10:g.128750540A>G , CM000670.1:g.128750540A>G	GRCh37
NC_000008.9:g.128819722A>G	NCBI36
NG_007161.1:g.7225A>G
NG_007161.2:g.7861A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000707113.1:c.32A>G	ENSP00000516742.1:p.Asn11Ser
ENST00000707114.1:c.32A>G	ENSP00000516743.1:p.Asn11Ser
ENST00000707115.1:c.32A>G	ENSP00000516744.1:p.Asn11Ser
ENST00000707116.1:c.32A>G	ENSP00000516745.1:p.Asn11Ser
ENST00000517291.2:c.74A>G	ENSP00000429441.2:p.Asn25Ser
ENST00000524013.2:c.74A>G	ENSP00000430235.2:p.Asn25Ser
ENST00000621592.8:c.77A>G MANE Select	ENSP00000478887.2:p.Asn26Ser
ENST00000651626.1:c.-269A>G	ENSP00000499182.1:n.-269A>G
ENST00000652288.1:c.32A>G	ENSP00000499105.1:p.Asn11Ser
ENST00000259523.10:c.32A>G	ENSP00000259523.6:p.Asn11Ser
ENST00000377970.6:c.32A>G	ENSP00000367207.3:p.Asn11Ser
ENST00000517291.1:c.74A>G	ENSP00000429441.1:p.Asn25Ser
ENST00000520751.1:c.-3A>G	ENSP00000430226.1:n.-3A>G
ENST00000524013.1:c.74A>G	ENSP00000430235.1:p.Asn25Ser
ENST00000613283.1:c.77A>G	ENSP00000479618.1:p.Asn26Ser
ENST00000621592.5:c.77A>G	ENSP00000478887.1:p.Asn26Ser
NM_002467.4:c.77A>G	NP_002458.2:p.Asn26Ser
NM_001354870.1:c.74A>G	NP_001341799.1:p.Asn25Ser
NM_002467.5:c.77A>G	NP_002458.2:p.Asn26Ser
NM_002467.6:c.77A>G MANE Select	NP_002458.2:p.Asn26Ser