Canonical Allele Identifier: CA470776231
Gene: MARK2P9 HGNC NCBI

Linked Data

dbSNP Id: rs2135255152
MyVariant Identifiers: chr10:g.94178676A>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.92418919A>G , CM000672.2:g.92418919A>G GRCh38
NC_000010.10:g.94178676A>G , CM000672.1:g.94178676A>G GRCh37
NC_000010.9:g.94168656A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000430958.1:n.253A>G
NR_038243.2:n.259A>G