Canonical Allele Identifier: CA470776419
Gene: MARK2P9 HGNC NCBI

Linked Data

dbSNP Id: rs1844379033
MyVariant Identifiers: chr10:g.94178742G>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.92418985G>A , CM000672.2:g.92418985G>A GRCh38
NC_000010.10:g.94178742G>A , CM000672.1:g.94178742G>A GRCh37
NC_000010.9:g.94168722G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000430958.1:n.319G>A
NR_038243.2:n.325G>A
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