Canonical Allele Identifier: CA345931737

Gene: MYCN

Linked Data

• dbSNP Id: rs2103330418
• MyVariant Identifiers: chr2:g.16085669T>A (hg19) ; chr2:g.15945547T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.15945547T>A , CM000664.2:g.15945547T>A	GRCh38
NC_000002.11:g.16085669T>A , CM000664.1:g.16085669T>A	GRCh37
NC_000002.10:g.16003120T>A	NCBI36
NG_007457.1:g.9987T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703162.1:n.194T>A
ENST00000281043.4:c.845T>A MANE Select	ENSP00000281043.3:p.Val282Glu
ENST00000638417.1:c.212T>A	ENSP00000491476.1:p.Val71Glu
ENST00000281043.3:c.845T>A	ENSP00000281043.3:p.Val282Glu
NM_001293228.1:c.845T>A	NP_001280157.1:p.Val282Glu
NM_001293231.1:c.212T>A	NP_001280160.1:p.Val71Glu
NM_001293233.1:c.*780T>A	NP_001280162.1:n.*780T>A
NM_005378.5:c.845T>A	NP_005369.2:p.Val282Glu
NM_005378.6:c.845T>A MANE Select	NP_005369.2:p.Val282Glu
NM_001293228.2:c.845T>A	NP_001280157.1:p.Val282Glu
NM_001293231.2:c.212T>A	NP_001280160.1:p.Val71Glu
NM_001293233.2:c.*780T>A	NP_001280162.1:n.*780T>A