Canonical Allele Identifier: CA470776250
Gene: MARK2P9 HGNC NCBI

Linked Data

dbSNP Id: rs1590693014
MyVariant Identifiers: chr10:g.94178683C>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.92418926C>G , CM000672.2:g.92418926C>G GRCh38
NC_000010.10:g.94178683C>G , CM000672.1:g.94178683C>G GRCh37
NC_000010.9:g.94168663C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000430958.1:n.260C>G
NR_038243.2:n.266C>G
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