Canonical Allele Identifier: CA470777216

Gene: MARK2P9

Linked Data

• dbSNP Id: rs1198455950
• gnomAD v2: 10-94179017-T-G
• gnomAD v3: 10-92419260-T-G
• gnomAD v4: 10-92419260-T-G
• MyVariant Identifiers: chr10:g.94179017T>G (hg19) ; chr10:g.92419260T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.92419260T>G , CM000672.2:g.92419260T>G	GRCh38
NC_000010.10:g.94179017T>G , CM000672.1:g.94179017T>G	GRCh37
NC_000010.9:g.94168997T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000430958.1:n.594T>G
NR_038243.2:n.600T>G