Canonical Allele Identifier: CA470776323

Gene: MARK2P9

Linked Data

• dbSNP Id: rs1590693022
• MyVariant Identifiers: chr10:g.94178708G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.92418951G>A , CM000672.2:g.92418951G>A	GRCh38
NC_000010.10:g.94178708G>A , CM000672.1:g.94178708G>A	GRCh37
NC_000010.9:g.94168688G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000430958.1:n.285G>A
NR_038243.2:n.291G>A