Canonical Allele Identifier: CA345931834

Gene: MYCN

Linked Data

• dbSNP Id: rs1662842475
• gnomAD v4: 2-15945594-A-G
• MyVariant Identifiers: chr2:g.16085716A>G (hg19) ; chr2:g.15945594A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.15945594A>G , CM000664.2:g.15945594A>G	GRCh38
NC_000002.11:g.16085716A>G , CM000664.1:g.16085716A>G	GRCh37
NC_000002.10:g.16003167A>G	NCBI36
NG_007457.1:g.10034A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703162.1:n.241A>G
ENST00000281043.4:c.892A>G MANE Select	ENSP00000281043.3:p.Thr298Ala
ENST00000638417.1:c.259A>G	ENSP00000491476.1:p.Thr87Ala
ENST00000281043.3:c.892A>G	ENSP00000281043.3:p.Thr298Ala
NM_001293228.1:c.892A>G	NP_001280157.1:p.Thr298Ala
NM_001293231.1:c.259A>G	NP_001280160.1:p.Thr87Ala
NM_001293233.1:c.*827A>G	NP_001280162.1:n.*827A>G
NM_005378.5:c.892A>G	NP_005369.2:p.Thr298Ala
NM_005378.6:c.892A>G MANE Select	NP_005369.2:p.Thr298Ala
NM_001293228.2:c.892A>G	NP_001280157.1:p.Thr298Ala
NM_001293231.2:c.259A>G	NP_001280160.1:p.Thr87Ala
NM_001293233.2:c.*827A>G	NP_001280162.1:n.*827A>G