ClinGen Allele Registry
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Canonical Allele Identifier:
CA1057439554
Gene: LINC02043
HGNC
NCBI
Linked Data
dbSNP Id:
rs1722608996
gnomAD v3:
3-186812648-T-C
gnomAD v4:
3-186812648-T-C
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000003.12:g.186812648T>C , CM000665.2:g.186812648T>C
GRCh38
NC_000003.11:g.186530437T>C , CM000665.1:g.186530437T>C
GRCh37
NC_000003.10:g.188013131T>C
NCBI36
Transcript Alleles
HGVS
Amino-acid Change
NR_125409.1:n.564-500A>G
Search 100 bp 5'
Search 100 bp 3'