Canonical Allele Identifier: CA211483463
Gene: MARK2P9 HGNC NCBI

Linked Data

dbSNP Id: rs190037794
gnomAD v3: 10-92418955-G-C
gnomAD v4: 10-92418955-G-C
MyVariant Identifiers: chr10:g.94178712G>C (hg19) chr10:g.92418955G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.92418955G>C , CM000672.2:g.92418955G>C GRCh38
NC_000010.10:g.94178712G>C , CM000672.1:g.94178712G>C GRCh37
NC_000010.9:g.94168692G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000430958.1:n.289G>C
NR_038243.2:n.295G>C
Search 100 bp 5'
Search 100 bp 3'