Canonical Allele Identifier: CA211483608
Gene: MARK2P9 HGNC NCBI

Linked Data

dbSNP Id: rs992269417
gnomAD v3: 10-92419095-C-G
gnomAD v4: 10-92419095-C-G
MyVariant Identifiers: chr10:g.94178852C>G (hg19) chr10:g.92419095C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.92419095C>G , CM000672.2:g.92419095C>G GRCh38
NC_000010.10:g.94178852C>G , CM000672.1:g.94178852C>G GRCh37
NC_000010.9:g.94168832C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000430958.1:n.429C>G
NR_038243.2:n.435C>G
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