Canonical Allele Identifier: CA345931889
Gene: MYCN HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.16085746C>A (hg19) chr2:g.15945624C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.15945624C>A , CM000664.2:g.15945624C>A GRCh38
NC_000002.11:g.16085746C>A , CM000664.1:g.16085746C>A GRCh37
NC_000002.10:g.16003197C>A NCBI36
NG_007457.1:g.10064C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000703162.1:n.271C>A
ENST00000281043.4:c.922C>A MANE Select ENSP00000281043.3:p.Leu308Met
ENST00000638417.1:c.289C>A ENSP00000491476.1:p.Leu97Met
ENST00000281043.3:c.922C>A ENSP00000281043.3:p.Leu308Met
NM_001293228.1:c.922C>A NP_001280157.1:p.Leu308Met
NM_001293231.1:c.289C>A NP_001280160.1:p.Leu97Met
NM_001293233.1:c.*857C>A NP_001280162.1:n.*857C>A
NM_005378.5:c.922C>A NP_005369.2:p.Leu308Met
NM_005378.6:c.922C>A MANE Select NP_005369.2:p.Leu308Met
NM_001293228.2:c.922C>A NP_001280157.1:p.Leu308Met
NM_001293231.2:c.289C>A NP_001280160.1:p.Leu97Met
NM_001293233.2:c.*857C>A NP_001280162.1:n.*857C>A
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