ClinGen Allele Registry
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Canonical Allele Identifier:
CA53081652
Gene: LINC01104
HGNC
NCBI
Linked Data
dbSNP Id:
rs1051329954
gnomAD v3:
2-100219246-G-A
gnomAD v4:
2-100219246-G-A
MyVariant Identifiers:
chr2:g.100835708G>A (hg19)
chr2:g.100219246G>A (hg38)
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000002.12:g.100219246G>A , CM000664.2:g.100219246G>A
GRCh38
NC_000002.11:g.100835708G>A , CM000664.1:g.100835708G>A
GRCh37
NC_000002.10:g.100202140G>A
NCBI36
Transcript Alleles
HGVS
Amino-acid Change
NR_103730.1:n.567+10426G>A
Search 100 bp 5'
Search 100 bp 3'