Canonical Allele Identifier: CA470776474
Gene: MARK2P9 HGNC NCBI

Linked Data

dbSNP Id: rs1564572934
MyVariant Identifiers: chr10:g.94178761G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.92419004G>A , CM000672.2:g.92419004G>A GRCh38
NC_000010.10:g.94178761G>A , CM000672.1:g.94178761G>A GRCh37
NC_000010.9:g.94168741G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000430958.1:n.338G>A
NR_038243.2:n.344G>A