ClinGen Allele Registry
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Canonical Allele Identifier:
CA660801791
Gene: LINC01153
HGNC
NCBI
Linked Data
dbSNP Id:
rs1332103641
gnomAD v3:
10-121179879-T-G
gnomAD v4:
10-121179879-T-G
MyVariant Identifiers:
chr10:g.122939393T>G (hg19)
chr10:g.121179879T>G (hg38)
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000010.11:g.121179879T>G , CM000672.2:g.121179879T>G
GRCh38
NC_000010.10:g.122939393T>G , CM000672.1:g.122939393T>G
GRCh37
NC_000010.9:g.122929383T>G
NCBI36
Transcript Alleles
HGVS
Amino-acid Change
XR_246197.2:n.684+907T>G
Search 100 bp 5'
Search 100 bp 3'