Canonical Allele Identifier: CA595637039
Gene: MARK2P9 HGNC NCBI

Linked Data

dbSNP Id: rs1236952954

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.92418998_92419000del , CM000672.2:g.92418998_92419000del GRCh38
NC_000010.10:g.94178755_94178757del , CM000672.1:g.94178755_94178757del GRCh37
NC_000010.9:g.94168735_94168737del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000430958.1:n.332_334del
NR_038243.2:n.338_340del