Canonical Allele Identifier: CA470776291

Gene: MARK2P9

Linked Data

• COSMIC: COSN222986
• MyVariant Identifiers: chr10:g.94178697G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.92418940G>C , CM000672.2:g.92418940G>C	GRCh38
NC_000010.10:g.94178697G>C , CM000672.1:g.94178697G>C	GRCh37
NC_000010.9:g.94168677G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000430958.1:n.274G>C
NR_038243.2:n.280G>C