Canonical Allele Identifier: CA43192101

Gene: MYCN MYCNOS

Linked Data

• dbSNP Id: rs886765376
• gnomAD v2: 2-16082227-G-A
• gnomAD v4: 2-15942105-G-A
• MyVariant Identifiers: chr2:g.16082227G>A (hg19) ; chr2:g.15942105G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.15942105G>A , CM000664.2:g.15942105G>A	GRCh38
NC_000002.11:g.16082227G>A , CM000664.1:g.16082227G>A	GRCh37
NC_000002.10:g.15999678G>A	NCBI36
NG_007457.1:g.6545G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000281043.4:c.41G>A (MYCN) MANE Select	ENSP00000281043.3:p.Cys14Tyr
ENST00000638417.1:c.157+1362G>A (MYCN)	ENSP00000491476.1:n.157+1362G>A
ENST00000281043.3:c.41G>A (MYCN)	ENSP00000281043.3:p.Cys14Tyr
NM_001293228.1:c.41G>A (MYCN)	NP_001280157.1:p.Cys14Tyr
NM_001293231.1:c.157+1362G>A (MYCN)	NP_001280160.1:n.157+1362G>A
NM_001293233.1:c.315G>A (MYCN)	NP_001280162.1:p.Leu105=
NM_005378.5:c.41G>A (MYCN)	NP_005369.2:p.Cys14Tyr
NM_001329968.1:c.-234+47C>T (MYCNOS)	NP_001316897.1:n.-234+47C>T
XM_024452528.1:c.-234+277C>T (MYCNOS)	XP_024308296.1:n.-234+277C>T
NM_005378.6:c.41G>A (MYCN) MANE Select	NP_005369.2:p.Cys14Tyr
NM_001293228.2:c.41G>A (MYCN)	NP_001280157.1:p.Cys14Tyr
NM_001293231.2:c.157+1362G>A (MYCN)	NP_001280160.1:n.157+1362G>A
NM_001293233.2:c.315G>A (MYCN)	NP_001280162.1:p.Leu105=
NR_161163.1:n.282+47C>T (MYCNOS)