Canonical Allele Identifier: CA211483528
Gene: MARK2P9 HGNC NCBI

Linked Data

dbSNP Id: rs546438202
gnomAD v3: 10-92418973-C-A
gnomAD v4: 10-92418973-C-A
MyVariant Identifiers: chr10:g.94178730C>A (hg19) chr10:g.92418973C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.92418973C>A , CM000672.2:g.92418973C>A GRCh38
NC_000010.10:g.94178730C>A , CM000672.1:g.94178730C>A GRCh37
NC_000010.9:g.94168710C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000430958.1:n.307C>A
NR_038243.2:n.313C>A
Search 100 bp 5'
Search 100 bp 3'