Canonical Allele Identifier: CA470776769
Gene: MARK2P9 HGNC NCBI

Linked Data

dbSNP Id: rs1396537907
gnomAD v3: 10-92419105-T-C
gnomAD v4: 10-92419105-T-C
MyVariant Identifiers: chr10:g.94178862T>C (hg19) chr10:g.92419105T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.92419105T>C , CM000672.2:g.92419105T>C GRCh38
NC_000010.10:g.94178862T>C , CM000672.1:g.94178862T>C GRCh37
NC_000010.9:g.94168842T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000430958.1:n.439T>C
NR_038243.2:n.445T>C
Search 100 bp 5'
Search 100 bp 3'