Canonical Allele Identifier: CA470776480
Gene: MARK2P9 HGNC NCBI

Linked Data

dbSNP Id: rs1262137112
gnomAD v3: 10-92419006-G-A
gnomAD v4: 10-92419006-G-A
MyVariant Identifiers: chr10:g.94178763G>A (hg19) chr10:g.92419006G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.92419006G>A , CM000672.2:g.92419006G>A GRCh38
NC_000010.10:g.94178763G>A , CM000672.1:g.94178763G>A GRCh37
NC_000010.9:g.94168743G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000430958.1:n.340G>A
NR_038243.2:n.346G>A
Search 100 bp 5'
Search 100 bp 3'