Canonical Allele Identifier: CA1538264
Gene: MYCN HGNC NCBI

Linked Data

dbSNP Id: rs762164859
gnomAD v2: 2-16085681-G-A
gnomAD v3: 2-15945559-G-A
gnomAD v4: 2-15945559-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.15945559G>A , CM000664.2:g.15945559G>A GRCh38
NC_000002.11:g.16085681G>A , CM000664.1:g.16085681G>A GRCh37
NC_000002.10:g.16003132G>A NCBI36
NG_007457.1:g.9999G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000703162.1:n.206G>A
ENST00000281043.4:c.857G>A MANE Select ENSP00000281043.3:p.Arg286His
ENST00000638417.1:c.224G>A ENSP00000491476.1:p.Arg75His
ENST00000281043.3:c.857G>A ENSP00000281043.3:p.Arg286His
NM_001293228.1:c.857G>A NP_001280157.1:p.Arg286His
NM_001293231.1:c.224G>A NP_001280160.1:p.Arg75His
NM_001293233.1:c.*792G>A NP_001280162.1:n.*792G>A
NM_005378.5:c.857G>A NP_005369.2:p.Arg286His
NM_005378.6:c.857G>A MANE Select NP_005369.2:p.Arg286His
NM_001293228.2:c.857G>A NP_001280157.1:p.Arg286His
NM_001293231.2:c.224G>A NP_001280160.1:p.Arg75His
NM_001293233.2:c.*792G>A NP_001280162.1:n.*792G>A