ClinGen Allele Registry
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Canonical Allele Identifier:
CA535050370
Gene: LINC01104
HGNC
NCBI
Linked Data
dbSNP Id:
rs1259284092
gnomAD v2:
2-100835689-A-G
gnomAD v3:
2-100219227-A-G
gnomAD v4:
2-100219227-A-G
MyVariant Identifiers:
chr2:g.100835689A>G (hg19)
chr2:g.100219227A>G (hg38)
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000002.12:g.100219227A>G , CM000664.2:g.100219227A>G
GRCh38
NC_000002.11:g.100835689A>G , CM000664.1:g.100835689A>G
GRCh37
NC_000002.10:g.100202121A>G
NCBI36
Transcript Alleles
HGVS
Amino-acid Change
NR_103730.1:n.567+10407A>G
Search 100 bp 5'
Search 100 bp 3'