Canonical Allele Identifier: CA211483604
Gene: MARK2P9 HGNC NCBI

Linked Data

dbSNP Id: rs960890813

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.92419088G>T , CM000672.2:g.92419088G>T GRCh38
NC_000010.10:g.94178845G>T , CM000672.1:g.94178845G>T GRCh37
NC_000010.9:g.94168825G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000430958.1:n.422G>T
NR_038243.2:n.428G>T