Canonical Allele Identifier: CA214889944
Gene: LINC01153 HGNC NCBI

Linked Data

dbSNP Id: rs182631961
gnomAD v3: 10-121179940-T-A
gnomAD v4: 10-121179940-T-A
MyVariant Identifiers: chr10:g.122939454T>A (hg19) chr10:g.121179940T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.121179940T>A , CM000672.2:g.121179940T>A GRCh38
NC_000010.10:g.122939454T>A , CM000672.1:g.122939454T>A GRCh37
NC_000010.9:g.122929444T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_246197.2:n.684+968T>A
Search 100 bp 5'
Search 100 bp 3'