Canonical Allele Identifier: CA470776402
Gene: MARK2P9 HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.94178736C>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.92418979C>G , CM000672.2:g.92418979C>G GRCh38
NC_000010.10:g.94178736C>G , CM000672.1:g.94178736C>G GRCh37
NC_000010.9:g.94168716C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000430958.1:n.313C>G
NR_038243.2:n.319C>G