Canonical Allele Identifier: CA470776528
Gene: MARK2P9 HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.94178779C>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.92419022C>G , CM000672.2:g.92419022C>G GRCh38
NC_000010.10:g.94178779C>G , CM000672.1:g.94178779C>G GRCh37
NC_000010.9:g.94168759C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000430958.1:n.356C>G
NR_038243.2:n.362C>G