Canonical Allele Identifier: CA15655676
Gene: LINC01153 HGNC NCBI

Linked Data

dbSNP Id: rs7085142
gnomAD v2: 10-122939374-T-C
gnomAD v3: 10-121179860-T-C
gnomAD v4: 10-121179860-T-C
MyVariant Identifiers: chr10:g.122939374T>C (hg19) chr10:g.121179860T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.121179860T>C , CM000672.2:g.121179860T>C GRCh38
NC_000010.10:g.122939374T>C , CM000672.1:g.122939374T>C GRCh37
NC_000010.9:g.122929364T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_246197.2:n.684+888T>C
Search 100 bp 5'
Search 100 bp 3'