Canonical Allele Identifier: CA1538282

Gene: MYCN

Linked Data

• ClinVar Variation Id: 377368
• ClinVar RCV Id: RCV000436958
• dbSNP Id: rs200236475
• ExAC: 2:16085759 G / A
• gnomAD v2: 2-16085759-G-A
• gnomAD v3: 2-15945637-G-A
• gnomAD v4: 2-15945637-G-A
• MyVariant Identifiers: chr2:g.16085759G>A (hg19) ; chr2:g.15945637G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.15945637G>A , CM000664.2:g.15945637G>A	GRCh38
NC_000002.11:g.16085759G>A , CM000664.1:g.16085759G>A	GRCh37
NC_000002.10:g.16003210G>A	NCBI36
NG_007457.1:g.10077G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703162.1:n.284G>A
ENST00000281043.4:c.935G>A MANE Select	ENSP00000281043.3:p.Arg312Lys
ENST00000638417.1:c.302G>A	ENSP00000491476.1:p.Arg101Lys
ENST00000281043.3:c.935G>A	ENSP00000281043.3:p.Arg312Lys
NM_001293228.1:c.935G>A	NP_001280157.1:p.Arg312Lys
NM_001293231.1:c.302G>A	NP_001280160.1:p.Arg101Lys
NM_001293233.1:c.*870G>A	NP_001280162.1:n.*870G>A
NM_005378.5:c.935G>A	NP_005369.2:p.Arg312Lys
NM_005378.6:c.935G>A MANE Select	NP_005369.2:p.Arg312Lys
NM_001293228.2:c.935G>A	NP_001280157.1:p.Arg312Lys
NM_001293231.2:c.302G>A	NP_001280160.1:p.Arg101Lys
NM_001293233.2:c.*870G>A	NP_001280162.1:n.*870G>A