Canonical Allele Identifier: CA1940871525
Gene: LINC01153 HGNC NCBI

Linked Data

dbSNP Id: rs1850760420
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.121179815A>C , CM000672.2:g.121179815A>C GRCh38
NC_000010.10:g.122939329A>C , CM000672.1:g.122939329A>C GRCh37
NC_000010.9:g.122929319A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_246197.2:n.684+843A>C
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