Canonical Allele Identifier: CA425092643

Gene: MYCN

Linked Data

• dbSNP Id: rs1359686492
• MyVariant Identifiers: chr2:g.16086003C>T (hg19) ; chr2:g.15945881C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.15945881C>T , CM000664.2:g.15945881C>T	GRCh38
NC_000002.11:g.16086003C>T , CM000664.1:g.16086003C>T	GRCh37
NC_000002.10:g.16003454C>T	NCBI36
NG_007457.1:g.10321C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000703162.1:n.528C>T
ENST00000281043.4:c.1179C>T MANE Select	ENSP00000281043.3:p.Arg393=
ENST00000638417.1:c.546C>T	ENSP00000491476.1:p.Arg182=
ENST00000281043.3:c.1179C>T	ENSP00000281043.3:p.Arg393=
NM_001293228.1:c.1179C>T	NP_001280157.1:p.Arg393=
NM_001293231.1:c.546C>T	NP_001280160.1:p.Arg182=
NM_001293233.1:c.*1114C>T	NP_001280162.1:n.*1114C>T
NM_005378.5:c.1179C>T	NP_005369.2:p.Arg393=
NM_005378.6:c.1179C>T MANE Select	NP_005369.2:p.Arg393=
NM_001293228.2:c.1179C>T	NP_001280157.1:p.Arg393=
NM_001293231.2:c.546C>T	NP_001280160.1:p.Arg182=
NM_001293233.2:c.*1114C>T	NP_001280162.1:n.*1114C>T