Canonical Allele Identifier: CA470776412
Gene: MARK2P9 HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.94178739A>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.92418982A>T , CM000672.2:g.92418982A>T GRCh38
NC_000010.10:g.94178739A>T , CM000672.1:g.94178739A>T GRCh37
NC_000010.9:g.94168719A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000430958.1:n.316A>T
NR_038243.2:n.322A>T
Search 100 bp 5'
Search 100 bp 3'