Canonical Allele Identifier: CA470777011
Gene: MARK2P9 HGNC NCBI

Linked Data

dbSNP Id: rs1316289205
MyVariant Identifiers: chr10:g.94178946A>G (hg19) chr10:g.92419189A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.92419189A>G , CM000672.2:g.92419189A>G GRCh38
NC_000010.10:g.94178946A>G , CM000672.1:g.94178946A>G GRCh37
NC_000010.9:g.94168926A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000430958.1:n.523A>G
NR_038243.2:n.529A>G
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