Canonical Allele Identifier: CA470776328
Gene: MARK2P9 HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.94178709A>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.92418952A>T , CM000672.2:g.92418952A>T GRCh38
NC_000010.10:g.94178709A>T , CM000672.1:g.94178709A>T GRCh37
NC_000010.9:g.94168689A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000430958.1:n.286A>T
NR_038243.2:n.292A>T