Canonical Allele Identifier: CA211483561

Gene: MARK2P9

Linked Data

• dbSNP Id: rs1025204772
• gnomAD v2: 10-94178776-C-G
• gnomAD v3: 10-92419019-C-G
• gnomAD v4: 10-92419019-C-G
• MyVariant Identifiers: chr10:g.94178776C>G (hg19) ; chr10:g.92419019C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.92419019C>G , CM000672.2:g.92419019C>G	GRCh38
NC_000010.10:g.94178776C>G , CM000672.1:g.94178776C>G	GRCh37
NC_000010.9:g.94168756C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000430958.1:n.353C>G
NR_038243.2:n.359C>G