Canonical Allele Identifier: CA470777319
Gene: MARK2P9 HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.94179054G>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.92419297G>C , CM000672.2:g.92419297G>C GRCh38
NC_000010.10:g.94179054G>C , CM000672.1:g.94179054G>C GRCh37
NC_000010.9:g.94169034G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000430958.1:n.631G>C
NR_038243.2:n.637G>C
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