Canonical Allele Identifier: CA2657954649
Gene: MYCN HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.15945503_15945511dup , CM000664.2:g.15945503_15945511dup GRCh38
NC_000002.11:g.16085625_16085633dup , CM000664.1:g.16085625_16085633dup GRCh37
NC_000002.10:g.16003076_16003084dup NCBI36
NG_007457.1:g.9943_9951dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000703162.1:n.150_158dup
ENST00000281043.4:c.801_809dup
ENST00000638417.1:c.168_176dup
ENST00000281043.3:c.801_809dup
NM_001293228.1:c.801_809dup
NM_001293231.1:c.168_176dup
NM_001293233.1:c.*736_*744dup
NM_005378.5:c.801_809dup
NM_005378.6:c.801_809dup
NM_001293228.2:c.801_809dup
NM_001293231.2:c.168_176dup
NM_001293233.2:c.*736_*744dup