Canonical Allele Identifier: CA1928171813
Gene: MARK2P9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.92419259G= , CM000672.2:g.92419259G= GRCh38
NC_000010.10:g.94179016G= , CM000672.1:g.94179016G= GRCh37
NC_000010.9:g.94168996G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000430958.1:n.593G=
NR_038243.2:n.599G=