Canonical Allele Identifier: CA470776261

Gene: MARK2P9

Linked Data

• dbSNP Id: rs1223077887
• MyVariant Identifiers: chr10:g.94178687A>C (hg19) ; chr10:g.92418930A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.92418930A>C , CM000672.2:g.92418930A>C	GRCh38
NC_000010.10:g.94178687A>C , CM000672.1:g.94178687A>C	GRCh37
NC_000010.9:g.94168667A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000430958.1:n.264A>C
NR_038243.2:n.270A>C