Canonical Allele Identifier: CA470776556
Gene: MARK2P9 HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.94178789G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.92419032G>A , CM000672.2:g.92419032G>A GRCh38
NC_000010.10:g.94178789G>A , CM000672.1:g.94178789G>A GRCh37
NC_000010.9:g.94168769G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000430958.1:n.366G>A
NR_038243.2:n.372G>A