Canonical Allele Identifier: CA211483567

Gene: MARK2P9

Linked Data

• dbSNP Id: rs904106041
• MyVariant Identifiers: chr10:g.94178786A>G (hg19) ; chr10:g.92419029A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.92419029A>G , CM000672.2:g.92419029A>G	GRCh38
NC_000010.10:g.94178786A>G , CM000672.1:g.94178786A>G	GRCh37
NC_000010.9:g.94168766A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000430958.1:n.363A>G
NR_038243.2:n.369A>G