Canonical Allele Identifier: CA211483438
Gene: MARK2P9 HGNC NCBI

Linked Data

dbSNP Id: rs745808189
gnomAD v2: 10-94178682-C-A
gnomAD v3: 10-92418925-C-A
gnomAD v4: 10-92418925-C-A
MyVariant Identifiers: chr10:g.94178682C>A (hg19) chr10:g.92418925C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.92418925C>A , CM000672.2:g.92418925C>A GRCh38
NC_000010.10:g.94178682C>A , CM000672.1:g.94178682C>A GRCh37
NC_000010.9:g.94168662C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000430958.1:n.259C>A
NR_038243.2:n.265C>A
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