Canonical Allele Identifier: CA470776245
Gene: MARK2P9 HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.94178681A>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.92418924A>C , CM000672.2:g.92418924A>C GRCh38
NC_000010.10:g.94178681A>C , CM000672.1:g.94178681A>C GRCh37
NC_000010.9:g.94168661A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000430958.1:n.258A>C
NR_038243.2:n.264A>C