Canonical Allele Identifier: CA345931928

Gene: MYCN

Linked Data

• MyVariant Identifiers: chr2:g.16085766G>C (hg19) ; chr2:g.15945644G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.15945644G>C , CM000664.2:g.15945644G>C	GRCh38
NC_000002.11:g.16085766G>C , CM000664.1:g.16085766G>C	GRCh37
NC_000002.10:g.16003217G>C	NCBI36
NG_007457.1:g.10084G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703162.1:n.291G>C
ENST00000281043.4:c.942G>C MANE Select	ENSP00000281043.3:p.Gln314His
ENST00000638417.1:c.309G>C	ENSP00000491476.1:p.Gln103His
ENST00000281043.3:c.942G>C	ENSP00000281043.3:p.Gln314His
NM_001293228.1:c.942G>C	NP_001280157.1:p.Gln314His
NM_001293231.1:c.309G>C	NP_001280160.1:p.Gln103His
NM_001293233.1:c.*877G>C	NP_001280162.1:n.*877G>C
NM_005378.5:c.942G>C	NP_005369.2:p.Gln314His
NM_005378.6:c.942G>C MANE Select	NP_005369.2:p.Gln314His
NM_001293228.2:c.942G>C	NP_001280157.1:p.Gln314His
NM_001293231.2:c.309G>C	NP_001280160.1:p.Gln103His
NM_001293233.2:c.*877G>C	NP_001280162.1:n.*877G>C