Canonical Allele Identifier: CA470776700

Gene: MARK2P9

Linked Data

• gnomAD v4: 10-92419080-C-T
• MyVariant Identifiers: chr10:g.94178837C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.92419080C>T , CM000672.2:g.92419080C>T	GRCh38
NC_000010.10:g.94178837C>T , CM000672.1:g.94178837C>T	GRCh37
NC_000010.9:g.94168817C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000430958.1:n.414C>T
NR_038243.2:n.420C>T