Canonical Allele Identifier: CA345932463

Gene: MYCN

Linked Data

• dbSNP Id: rs2103331590
• MyVariant Identifiers: chr2:g.16086011A>T (hg19) ; chr2:g.15945889A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.15945889A>T , CM000664.2:g.15945889A>T	GRCh38
NC_000002.11:g.16086011A>T , CM000664.1:g.16086011A>T	GRCh37
NC_000002.10:g.16003462A>T	NCBI36
NG_007457.1:g.10329A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000703162.1:n.536A>T
ENST00000281043.4:c.1187A>T MANE Select	ENSP00000281043.3:p.Asp396Val
ENST00000638417.1:c.554A>T	ENSP00000491476.1:p.Asp185Val
ENST00000281043.3:c.1187A>T	ENSP00000281043.3:p.Asp396Val
NM_001293228.1:c.1187A>T	NP_001280157.1:p.Asp396Val
NM_001293231.1:c.554A>T	NP_001280160.1:p.Asp185Val
NM_001293233.1:c.*1122A>T	NP_001280162.1:n.*1122A>T
NM_005378.5:c.1187A>T	NP_005369.2:p.Asp396Val
NM_005378.6:c.1187A>T MANE Select	NP_005369.2:p.Asp396Val
NM_001293228.2:c.1187A>T	NP_001280157.1:p.Asp396Val
NM_001293231.2:c.554A>T	NP_001280160.1:p.Asp185Val
NM_001293233.2:c.*1122A>T	NP_001280162.1:n.*1122A>T