Canonical Allele Identifier: CA211483698

Gene: MARK2P9

Linked Data

• dbSNP Id: rs895081515
• gnomAD v3: 10-92419242-G-C
• gnomAD v4: 10-92419242-G-C
• MyVariant Identifiers: chr10:g.94178999G>C (hg19) ; chr10:g.92419242G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.92419242G>C , CM000672.2:g.92419242G>C	GRCh38
NC_000010.10:g.94178999G>C , CM000672.1:g.94178999G>C	GRCh37
NC_000010.9:g.94168979G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000430958.1:n.576G>C
NR_038243.2:n.582G>C