Canonical Allele Identifier: CA345932451

Gene: MYCN

Linked Data

• dbSNP Id: rs104893648
• MyVariant Identifiers: chr2:g.16086005G>C (hg19) ; chr2:g.15945883G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.15945883G>C , CM000664.2:g.15945883G>C	GRCh38
NC_000002.11:g.16086005G>C , CM000664.1:g.16086005G>C	GRCh37
NC_000002.10:g.16003456G>C	NCBI36
NG_007457.1:g.10323G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000703162.1:n.530G>C
ENST00000281043.4:c.1181G>C MANE Select	ENSP00000281043.3:p.Arg394Pro
ENST00000638417.1:c.548G>C	ENSP00000491476.1:p.Arg183Pro
ENST00000281043.3:c.1181G>C	ENSP00000281043.3:p.Arg394Pro
NM_001293228.1:c.1181G>C	NP_001280157.1:p.Arg394Pro
NM_001293231.1:c.548G>C	NP_001280160.1:p.Arg183Pro
NM_001293233.1:c.*1116G>C	NP_001280162.1:n.*1116G>C
NM_005378.5:c.1181G>C	NP_005369.2:p.Arg394Pro
NM_005378.6:c.1181G>C MANE Select	NP_005369.2:p.Arg394Pro
NM_001293228.2:c.1181G>C	NP_001280157.1:p.Arg394Pro
NM_001293231.2:c.548G>C	NP_001280160.1:p.Arg183Pro
NM_001293233.2:c.*1116G>C	NP_001280162.1:n.*1116G>C