Canonical Allele Identifier: CA345931709

Gene: MYCN

Linked Data

• dbSNP Id: rs373661257
• MyVariant Identifiers: chr2:g.16085655C>G (hg19) ; chr2:g.15945533C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.15945533C>G , CM000664.2:g.15945533C>G	GRCh38
NC_000002.11:g.16085655C>G , CM000664.1:g.16085655C>G	GRCh37
NC_000002.10:g.16003106C>G	NCBI36
NG_007457.1:g.9973C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703162.1:n.180C>G
ENST00000281043.4:c.831C>G MANE Select	ENSP00000281043.3:p.Ile277Met
ENST00000638417.1:c.198C>G	ENSP00000491476.1:p.Ile66Met
ENST00000281043.3:c.831C>G	ENSP00000281043.3:p.Ile277Met
NM_001293228.1:c.831C>G	NP_001280157.1:p.Ile277Met
NM_001293231.1:c.198C>G	NP_001280160.1:p.Ile66Met
NM_001293233.1:c.*766C>G	NP_001280162.1:n.*766C>G
NM_005378.5:c.831C>G	NP_005369.2:p.Ile277Met
NM_005378.6:c.831C>G MANE Select	NP_005369.2:p.Ile277Met
NM_001293228.2:c.831C>G	NP_001280157.1:p.Ile277Met
NM_001293231.2:c.198C>G	NP_001280160.1:p.Ile66Met
NM_001293233.2:c.*766C>G	NP_001280162.1:n.*766C>G