Canonical Allele Identifier: CA2657954641

Gene: MYCN

Linked Data

• gnomAD v4: 2-15945455-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.15945455T>C , CM000664.2:g.15945455T>C	GRCh38
NC_000002.11:g.16085577T>C , CM000664.1:g.16085577T>C	GRCh37
NC_000002.10:g.16003028T>C	NCBI36
NG_007457.1:g.9895T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703162.1:n.140-38T>C
ENST00000281043.4:c.791-38T>C MANE Select	ENSP00000281043.3:n.791-38T>C
ENST00000638417.1:c.158-38T>C	ENSP00000491476.1:n.158-38T>C
ENST00000281043.3:c.791-38T>C	ENSP00000281043.3:n.791-38T>C
NM_001293228.1:c.791-38T>C	NP_001280157.1:n.791-38T>C
NM_001293231.1:c.158-38T>C	NP_001280160.1:n.158-38T>C
NM_001293233.1:c.*726-38T>C	NP_001280162.1:n.*726-38T>C
NM_005378.5:c.791-38T>C	NP_005369.2:n.791-38T>C
NM_005378.6:c.791-38T>C MANE Select	NP_005369.2:n.791-38T>C
NM_001293228.2:c.791-38T>C	NP_001280157.1:n.791-38T>C
NM_001293231.2:c.158-38T>C	NP_001280160.1:n.158-38T>C
NM_001293233.2:c.*726-38T>C	NP_001280162.1:n.*726-38T>C