Canonical Allele Identifier: CA211483557
Gene: MARK2P9 HGNC NCBI

Linked Data

dbSNP Id: rs774541452
gnomAD v2: 10-94178746-G-A
gnomAD v3: 10-92418989-G-A
gnomAD v4: 10-92418989-G-A
MyVariant Identifiers: chr10:g.94178746G>A (hg19) chr10:g.92418989G>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.92418989G>A , CM000672.2:g.92418989G>A GRCh38
NC_000010.10:g.94178746G>A , CM000672.1:g.94178746G>A GRCh37
NC_000010.9:g.94168726G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000430958.1:n.323G>A
NR_038243.2:n.329G>A
Search 100 bp 5'
Search 100 bp 3'