Canonical Allele Identifier: CA2589166946
Gene: LINC01153 HGNC NCBI

Linked Data

dbSNP Id: rs995352690
gnomAD v3: 10-121179885-C-T
gnomAD v4: 10-121179885-C-T
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Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid Change
XR_246197.2:n.684+913C>T
Search 100 bp 5'
Search 100 bp 3'