Canonical Allele Identifier: CA470776495

Gene: MARK2P9

Linked Data

• dbSNP Id: rs1199893801
• gnomAD v3: 10-92419011-C-A
• gnomAD v4: 10-92419011-C-A
• MyVariant Identifiers: chr10:g.94178768C>A (hg19) ; chr10:g.92419011C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.92419011C>A , CM000672.2:g.92419011C>A	GRCh38
NC_000010.10:g.94178768C>A , CM000672.1:g.94178768C>A	GRCh37
NC_000010.9:g.94168748C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000430958.1:n.345C>A
NR_038243.2:n.351C>A