Canonical Allele Identifier: CA1928171785
Gene: MARK2P9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.92419162T= , CM000672.2:g.92419162T= GRCh38
NC_000010.10:g.94178919T= , CM000672.1:g.94178919T= GRCh37
NC_000010.9:g.94168899T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000430958.1:n.496T=
NR_038243.2:n.502T=