Canonical Allele Identifier: CA470776455
Gene: MARK2P9 HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.94178754G>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.92418997G>C , CM000672.2:g.92418997G>C GRCh38
NC_000010.10:g.94178754G>C , CM000672.1:g.94178754G>C GRCh37
NC_000010.9:g.94168734G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000430958.1:n.331G>C
NR_038243.2:n.337G>C
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