Canonical Allele Identifier: CA470776637
Gene: MARK2P9 HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.94178816T>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.92419059T>A , CM000672.2:g.92419059T>A GRCh38
NC_000010.10:g.94178816T>A , CM000672.1:g.94178816T>A GRCh37
NC_000010.9:g.94168796T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000430958.1:n.393T>A
NR_038243.2:n.399T>A