Canonical Allele Identifier: CA425092518

Gene: MYCN

Linked Data

• dbSNP Id: rs1662844500
• MyVariant Identifiers: chr2:g.16085748G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.15945626G>A , CM000664.2:g.15945626G>A	GRCh38
NC_000002.11:g.16085748G>A , CM000664.1:g.16085748G>A	GRCh37
NC_000002.10:g.16003199G>A	NCBI36
NG_007457.1:g.10066G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703162.1:n.273G>A
ENST00000281043.4:c.924G>A MANE Select	ENSP00000281043.3:p.Leu308=
ENST00000638417.1:c.291G>A	ENSP00000491476.1:p.Leu97=
ENST00000281043.3:c.924G>A	ENSP00000281043.3:p.Leu308=
NM_001293228.1:c.924G>A	NP_001280157.1:p.Leu308=
NM_001293231.1:c.291G>A	NP_001280160.1:p.Leu97=
NM_001293233.1:c.*859G>A	NP_001280162.1:n.*859G>A
NM_005378.5:c.924G>A	NP_005369.2:p.Leu308=
NM_005378.6:c.924G>A MANE Select	NP_005369.2:p.Leu308=
NM_001293228.2:c.924G>A	NP_001280157.1:p.Leu308=
NM_001293231.2:c.291G>A	NP_001280160.1:p.Leu97=
NM_001293233.2:c.*859G>A	NP_001280162.1:n.*859G>A