Canonical Allele Identifier: CA470776404
Gene: MARK2P9 HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.94178737A>C (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.92418980A>C , CM000672.2:g.92418980A>C GRCh38
NC_000010.10:g.94178737A>C , CM000672.1:g.94178737A>C GRCh37
NC_000010.9:g.94168717A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000430958.1:n.314A>C
NR_038243.2:n.320A>C
Search 100 bp 5'
Search 100 bp 3'