Canonical Allele Identifier: CA531217880

Gene: MYCN

Linked Data

• dbSNP Id: rs1439151628
• gnomAD v2: 2-16085613-AGATGATGAAGAT-A
• gnomAD v4: 2-15945491-AGATGATGAAGAT-A
• MyVariant Identifiers: chr2:g.16085614_16085625del (hg19) ; chr2:g.15945492_15945503del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.15945497_15945508del , CM000664.2:g.15945497_15945508del	GRCh38
NC_000002.11:g.16085619_16085630del , CM000664.1:g.16085619_16085630del	GRCh37
NC_000002.10:g.16003070_16003081del	NCBI36
NG_007457.1:g.9937_9948del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703162.1:n.144_155del
ENST00000281043.4:c.795_806del
ENST00000638417.1:c.162_173del
ENST00000281043.3:c.795_806del
NM_001293228.1:c.795_806del
NM_001293231.1:c.162_173del
NM_001293233.1:c.*730_*741del
NM_005378.5:c.795_806del
NM_005378.6:c.795_806del
NM_001293228.2:c.795_806del
NM_001293231.2:c.162_173del
NM_001293233.2:c.*730_*741del