Canonical Allele Identifier: CA470777270
Gene: MARK2P9 HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.94179037G>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.92419280G>T , CM000672.2:g.92419280G>T GRCh38
NC_000010.10:g.94179037G>T , CM000672.1:g.94179037G>T GRCh37
NC_000010.9:g.94169017G>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000430958.1:n.614G>T
NR_038243.2:n.620G>T