Canonical Allele Identifier: CA211483635

Gene: MARK2P9

Linked Data

• dbSNP Id: rs989094981
• MyVariant Identifiers: chr10:g.94178917G>A (hg19) ; chr10:g.92419160G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.92419160G>A , CM000672.2:g.92419160G>A	GRCh38
NC_000010.10:g.94178917G>A , CM000672.1:g.94178917G>A	GRCh37
NC_000010.9:g.94168897G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000430958.1:n.494G>A
NR_038243.2:n.500G>A