Canonical Allele Identifier: CA470777049

Gene: MARK2P9

Linked Data

• gnomAD v4: 10-92419202-T-C
• MyVariant Identifiers: chr10:g.94178959T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.92419202T>C , CM000672.2:g.92419202T>C	GRCh38
NC_000010.10:g.94178959T>C , CM000672.1:g.94178959T>C	GRCh37
NC_000010.9:g.94168939T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000430958.1:n.536T>C
NR_038243.2:n.542T>C