Canonical Allele Identifier: CA214889936
Gene: LINC01153 HGNC NCBI

Linked Data

dbSNP Id: rs995352690
MyVariant Identifiers: chr10:g.122939399C>G (hg19) chr10:g.121179885C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.121179885C>G , CM000672.2:g.121179885C>G GRCh38
NC_000010.10:g.122939399C>G , CM000672.1:g.122939399C>G GRCh37
NC_000010.9:g.122929389C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_246197.2:n.684+913C>G
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