Canonical Allele Identifier: CA211483514
Gene: MARK2P9 HGNC NCBI

Linked Data

dbSNP Id: rs539748064
gnomAD v3: 10-92418967-T-A
gnomAD v4: 10-92418967-T-A
MyVariant Identifiers: chr10:g.94178724T>A (hg19) chr10:g.92418967T>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.92418967T>A , CM000672.2:g.92418967T>A GRCh38
NC_000010.10:g.94178724T>A , CM000672.1:g.94178724T>A GRCh37
NC_000010.9:g.94168704T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000430958.1:n.301T>A
NR_038243.2:n.307T>A
Search 100 bp 5'
Search 100 bp 3'