Canonical Allele Identifier: CA211483554
Gene: MARK2P9 HGNC NCBI

Linked Data

dbSNP Id: rs182596626
gnomAD v2: 10-94178731-C-T
gnomAD v3: 10-92418974-C-T
gnomAD v4: 10-92418974-C-T
MyVariant Identifiers: chr10:g.94178731C>T (hg19) chr10:g.92418974C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.92418974C>T , CM000672.2:g.92418974C>T GRCh38
NC_000010.10:g.94178731C>T , CM000672.1:g.94178731C>T GRCh37
NC_000010.9:g.94168711C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000430958.1:n.308C>T
NR_038243.2:n.314C>T
Search 100 bp 5'
Search 100 bp 3'