Canonical Allele Identifier: CA470776720
Gene: MARK2P9 HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.94178845G>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.92419088G>A , CM000672.2:g.92419088G>A GRCh38
NC_000010.10:g.94178845G>A , CM000672.1:g.94178845G>A GRCh37
NC_000010.9:g.94168825G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000430958.1:n.422G>A
NR_038243.2:n.428G>A
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