Canonical Allele Identifier: CA13199015
Gene: MARK2P9 HGNC NCBI
MyVariant.info:
GRCh38 chr10:g.92419271C>T
GRCh37 chr10:g.94179028C>T
gnomAD v2:
10:94179028 C / T
gnomAD v3:
10:92419271 C / T
gnomAD v4:
chr10-92419271-C-T
Joint Max Group AF 0.74481824 (EAS)
Genomes Max Group AF 0.74481824 (EAS)
Exomes Max Group AF 0.17768 (AMR)
dbSNP:
2209972
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.92419271C>T , CM000672.2:g.92419271C>T GRCh38
NC_000010.10:g.94179028C>T , CM000672.1:g.94179028C>T GRCh37
NC_000010.9:g.94169008C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000430958.1:n.605C>T
NR_038243.2:n.611C>T
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