Canonical Allele Identifier: CA470776752
Gene: MARK2P9 HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.94178856A>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.92419099A>G , CM000672.2:g.92419099A>G GRCh38
NC_000010.10:g.94178856A>G , CM000672.1:g.94178856A>G GRCh37
NC_000010.9:g.94168836A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000430958.1:n.433A>G
NR_038243.2:n.439A>G