Canonical Allele Identifier: CA470776837
Gene: MARK2P9 HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.94178885T>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.92419128T>G , CM000672.2:g.92419128T>G GRCh38
NC_000010.10:g.94178885T>G , CM000672.1:g.94178885T>G GRCh37
NC_000010.9:g.94168865T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000430958.1:n.462T>G
NR_038243.2:n.468T>G