Canonical Allele Identifier: CA470776279
Gene: MARK2P9 HGNC NCBI

Linked Data

dbSNP Id: rs1281273881
gnomAD v2: 10-94178693-T-C
gnomAD v3: 10-92418936-T-C
gnomAD v4: 10-92418936-T-C
MyVariant Identifiers: chr10:g.94178693T>C (hg19) chr10:g.92418936T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.92418936T>C , CM000672.2:g.92418936T>C GRCh38
NC_000010.10:g.94178693T>C , CM000672.1:g.94178693T>C GRCh37
NC_000010.9:g.94168673T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000430958.1:n.270T>C
NR_038243.2:n.276T>C
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