ClinGen Allele Registry
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Canonical Allele Identifier:
CA1110699995
Gene: LINC00208
HGNC
NCBI
Linked Data
dbSNP Id:
rs1802023393
gnomAD v3:
8-11577789-A-G
gnomAD v4:
8-11577789-A-G
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000008.11:g.11577789A>G , CM000670.2:g.11577789A>G
GRCh38
NC_000008.10:g.11435298A>G , CM000670.1:g.11435298A>G
GRCh37
NC_000008.9:g.11472707A>G
NCBI36
Transcript Alleles
HGVS
Amino-acid Change
NR_040035.1:n.783+472A>G
Search 100 bp 5'
Search 100 bp 3'