Canonical Allele Identifier: CA669987489
Gene: MARK2P9 HGNC NCBI

Linked Data

dbSNP Id: rs1406006391
gnomAD v3: 10-92419081-CA-C
gnomAD v4: 10-92419081-CA-C
MyVariant Identifiers: chr10:g.94178839del (hg19) chr10:g.92419082del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.92419082del , CM000672.2:g.92419082del GRCh38
NC_000010.10:g.94178839del , CM000672.1:g.94178839del GRCh37
NC_000010.9:g.94168819del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000430958.1:n.416del
NR_038243.2:n.422del
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