Canonical Allele Identifier: CA470776686
Gene: MARK2P9 HGNC NCBI

Linked Data

dbSNP Id: rs1220653515
gnomAD v4: 10-92419076-G-A
MyVariant Identifiers: chr10:g.94178833G>A (hg19) chr10:g.92419076G>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.92419076G>A , CM000672.2:g.92419076G>A GRCh38
NC_000010.10:g.94178833G>A , CM000672.1:g.94178833G>A GRCh37
NC_000010.9:g.94168813G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000430958.1:n.410G>A
NR_038243.2:n.416G>A
Search 100 bp 5'
Search 100 bp 3'